Transcript #00000024 (NM_001103.2, ACTN2 gene)

Transcript name actinin, alpha 2 (expired, new version available)
Gene name ACTN2 (actinin, alpha 2)
Chromosome 1
Transcript - NCBI ID NM_001103.2
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

78 entries on 1 page. Showing entries 1 - 78.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 01 c.26A>G - p.Gln9Arg
./. 01 c.26A>G - p.Gln9Arg
./. 02 c.241+33T>G - -
./. 03 c.244G>A - p.Glu82Lys
./. 03 c.301A>G - p.Asn101Asp
./. 03 c.331G>A - p.Gly111Arg
./. 03 c.332G>T - p.Gly111Val
./. 03 c.332G>T - p.Gly111Val
./. 03 c.355G>A - p.Ala119Thr
./. 03 c.355G>A - p.Ala119Thr
./. 04 c.378T>C - p.Asn126Asn
./. 04 c.448+73G>A - -
./. 05 c.508A>C - p.Asn170His
./. 05 c.536+10C>T - -
./. 07 c.617A>G - p.Asp206Gly
./. 07 c.686T>G - p.Leu229Trp
./. 07 c.690T>A - p.Asp230Glu
./. 07 c.697+34A>G - -
./. 08 c.705G>C - p.Val235Val
./. 08 c.783+23G>C - -
./. 09 c.876+41G>T - -
./. 10 c.877-48A>C - -
./. 10 c.877-42C>T - -
./. 10 c.893G>A - p.Arg298His
./. 10 c.899C>T - p.Thr300Met
./. 10 c.920G>A - p.Arg307Gln
./. 10 c.926C>T - p.Pro309Leu
./. 10 c.983G>A - p.Arg328Gln
./. 10 c.1057C>G - p.Arg353Gly
./. 11 c.1108-8C>G - -
./. 11 c.1115C>G - p.Ala372Gly
./. 11 c.1192C>T - p.Arg398Cys
./. 11 c.1235C>T - p.Thr412Met
./. 12 c.1292C>T - p.Ser431Leu
./. 12 c.1298C>T - p.Ser433Leu
./. 12 c.1341C>T - p.Phe447Phe
./. 13 c.1423G>A - p.Asp475Asn
./. 13 c.1426G>A - p.Ala476Thr
./. 13 c.1484C>T - p.Thr495Met
./. 13 c.1484C>T - p.Thr495Met
./. 13 c.1513G>T - p.Glu505X
./. 13 c.1515+48T>C - -
./. 13 c.1515+62A>G - -
./. 14 c.1519A>G - p.Met507Val
./. 14 c.1646A>T - p.Glu549Val
./. 14 c.1654C>A - p.Gln552Lys
./. 15 c.1714C>T - p.Arg572Trp
./. 15 c.1715G>A - p.Arg572Gln
./. 15 c.1748A>C - p.Glu583Ala
./. 15 c.1810A>G - p.Met604Val
./. 15 c.1810A>G - p.Met604Val
./. 16 c.1840-28delTTG - -
./. 16 c.1864G>A - p.Asp622Asn
./. 16 c.1883A>G - p.Glu628Gly
./. 16 c.1930G>A - p.Ala644Thr
./. 16 c.1930G>A - p.Ala644Thr
./. 16 c.1946T>C - p.Ile649Thr
./. 17 c.1984C>T - p.Arg662Trp
./. 17 c.2063A>G - p.Tyr688Cys
./. 17 c.2139G>C - p.Thr713Thr
./. 17 c.2143T>C - p.Tyr715His
./. 18 c.2161C>A - p.Arg721Ser
./. 18 c.2237A>G - p.Asp746Gly
./. 18 c.2252C>T - p.Thr751Ile
./. 18 c.2276G>C - p.Arg759Thr
./. 19 c.2302-30A>G - -
./. 19 c.2324A>T - p.His775Leu
./. 20 c.2377G>A - p.Glu793Lys
./. 20 c.2423C>T - p.Thr808Ile
./. 20 c.2468C>T - p.Ala823Val
./. 20 c.2488C>A - p.Gln830Lys
./. 20 c.2526+34G>G - -
./. 21 c.2551C>T - p.Arg851Cys
./. 21 c.2602G>A - p.Ala868Thr
./. 21 c.2610G>C - p.Ser870Ser
./. 21 c.2639A>C - p.Asp880Ala
./. 21 c.2659G>A - p.Ala887Thr
./. 21 c.2677G>A - p.Asp893Asn
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