Canonical Allele Identifier: CA401459215

Gene: ACTG1

Linked Data

• MyVariant Identifiers: chr17:g.79478063C>G (hg19) ; chr17:g.81511037C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511037C>G , CM000679.2:g.81511037C>G	GRCh38
NC_000017.10:g.79478063C>G , CM000679.1:g.79478063C>G	GRCh37
NC_000017.9:g.77092658C>G	NCBI36
NG_011433.1:g.6765G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.874G>C	ENSP00000466346.2:p.Asp292His
ENST00000571691.6:c.802G>C	ENSP00000461407.2:p.Asp268His
ENST00000571721.6:c.874G>C	ENSP00000460660.2:p.Asp292His
ENST00000572105.7:c.*318G>C	ENSP00000462823.1:n.*318G>C
ENST00000573283.7:c.874G>C MANE Select	ENSP00000458435.1:p.Asp292His
ENST00000574671.6:n.1274G>C
ENST00000575659.6:c.874G>C	ENSP00000459119.2:p.Asp292His
ENST00000575994.6:c.874G>C	ENSP00000460464.2:p.Asp292His
ENST00000576214.3:n.1175G>C
ENST00000576544.6:c.874G>C	ENSP00000461672.1:p.Asp292His
ENST00000615544.5:c.874G>C	ENSP00000477968.1:p.Asp292His
ENST00000644774.2:c.847G>C	ENSP00000493648.2:p.Asp283His
ENST00000679410.1:n.1077G>C
ENST00000679480.1:c.874G>C	ENSP00000506201.1:p.Asp292His
ENST00000679535.1:n.1175G>C
ENST00000679778.1:c.874G>C	ENSP00000505235.1:p.Asp292His
ENST00000680227.1:c.874G>C	ENSP00000506253.1:p.Asp292His
ENST00000680727.1:c.874G>C	ENSP00000505193.1:p.Asp292His
ENST00000681052.1:c.874G>C	ENSP00000505060.1:p.Asp292His
ENST00000681092.1:c.*678G>C	ENSP00000506720.1:n.*678G>C
ENST00000681842.1:c.874G>C	ENSP00000506126.1:p.Asp292His
ENST00000331925.6:c.874G>C	ENSP00000331514.2:p.Asp292His
ENST00000572105.6:c.*318G>C	ENSP00000462823.1:n.*318G>C
ENST00000573283.5:c.874G>C	ENSP00000458435.1:p.Asp292His
ENST00000574671.5:n.733G>C
ENST00000575087.5:c.874G>C	ENSP00000459124.1:p.Asp292His
ENST00000575842.5:c.874G>C	ENSP00000458162.1:p.Asp292His
ENST00000576209.5:n.759G>C
ENST00000576544.5:c.874G>C	ENSP00000461672.1:p.Asp292His
ENST00000576917.5:n.1006G>C
ENST00000615544.4:c.874G>C	ENSP00000477968.1:p.Asp292His
NM_001199954.1:c.874G>C	NP_001186883.1:p.Asp292His
NM_001614.3:c.874G>C	NP_001605.1:p.Asp292His
NR_037688.1:n.1013G>C
NM_001199954.2:c.874G>C	NP_001186883.1:p.Asp292His
NM_001614.4:c.874G>C	NP_001605.1:p.Asp292His
NR_037688.2:n.946G>C
NM_001614.5:c.874G>C MANE Select	NP_001605.1:p.Asp292His
NR_037688.3:n.946G>C
NM_001199954.3:c.874G>C	NP_001186883.1:p.Asp292His