Canonical Allele Identifier: CA401460335
Gene: ACTG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1176366
ClinVar RCV Id: RCV001531873
dbSNP Id: rs2143777933

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81511356T>C , CM000679.2:g.81511356T>C GRCh38
NC_000017.10:g.79478382T>C , CM000679.1:g.79478382T>C GRCh37
NC_000017.9:g.77092977T>C NCBI36
NG_011433.1:g.6446A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000570382.2:c.634A>G ENSP00000466346.2:p.Ile212Val
ENST00000571691.6:c.562A>G ENSP00000461407.2:p.Ile188Val
ENST00000571721.6:c.634A>G ENSP00000460660.2:p.Ile212Val
ENST00000572105.7:c.*78A>G ENSP00000462823.1:n.*78A>G
ENST00000573283.7:c.634A>G MANE Select ENSP00000458435.1:p.Ile212Val
ENST00000574671.6:n.1034A>G
ENST00000575659.6:c.634A>G ENSP00000459119.2:p.Ile212Val
ENST00000575994.6:c.634A>G ENSP00000460464.2:p.Ile212Val
ENST00000576214.3:n.935A>G
ENST00000576544.6:c.634A>G ENSP00000461672.1:p.Ile212Val
ENST00000615544.5:c.634A>G ENSP00000477968.1:p.Ile212Val
ENST00000644774.2:c.607A>G ENSP00000493648.2:p.Ile203Val
ENST00000679410.1:n.758A>G
ENST00000679480.1:c.634A>G ENSP00000506201.1:p.Ile212Val
ENST00000679535.1:n.935A>G
ENST00000679778.1:c.634A>G ENSP00000505235.1:p.Ile212Val
ENST00000680227.1:c.634A>G ENSP00000506253.1:p.Ile212Val
ENST00000680727.1:c.634A>G ENSP00000505193.1:p.Ile212Val
ENST00000681052.1:c.634A>G ENSP00000505060.1:p.Ile212Val
ENST00000681092.1:c.*438A>G ENSP00000506720.1:n.*438A>G
ENST00000681842.1:c.634A>G ENSP00000506126.1:p.Ile212Val
ENST00000331925.6:c.634A>G ENSP00000331514.2:p.Ile212Val
ENST00000571691.5:c.607A>G ENSP00000461407.1:p.Ile203Val
ENST00000572105.6:c.*78A>G ENSP00000462823.1:n.*78A>G
ENST00000573283.5:c.634A>G ENSP00000458435.1:p.Ile212Val
ENST00000574671.5:n.493A>G
ENST00000575087.5:c.634A>G ENSP00000459124.1:p.Ile212Val
ENST00000575659.5:c.634A>G ENSP00000459119.1:p.Ile212Val
ENST00000575842.5:c.634A>G ENSP00000458162.1:p.Ile212Val
ENST00000575994.5:c.634A>G ENSP00000460464.1:p.Ile212Val
ENST00000576209.5:n.519A>G
ENST00000576214.2:n.832A>G
ENST00000576544.5:c.634A>G ENSP00000461672.1:p.Ile212Val
ENST00000576917.5:n.687A>G
ENST00000615544.4:c.634A>G ENSP00000477968.1:p.Ile212Val
NM_001199954.1:c.634A>G NP_001186883.1:p.Ile212Val
NM_001614.3:c.634A>G NP_001605.1:p.Ile212Val
NR_037688.1:n.773A>G
NM_001199954.2:c.634A>G NP_001186883.1:p.Ile212Val
NM_001614.4:c.634A>G NP_001605.1:p.Ile212Val
NR_037688.2:n.706A>G
NM_001614.5:c.634A>G MANE Select NP_001605.1:p.Ile212Val
NR_037688.3:n.706A>G
NM_001199954.3:c.634A>G NP_001186883.1:p.Ile212Val