Canonical Allele Identifier: CA245195

Gene: ACTG1

Linked Data

• ClinVar Variation Id: 197198
• ClinVar RCV Id: RCV000178166 ; RCV001267567 ; RCV002247591
• dbSNP Id: rs797044730
• MyVariant Identifiers: chr17:g.79478474G>A (hg19) ; chr17:g.81511448G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511448G>A , CM000679.2:g.81511448G>A	GRCh38
NC_000017.10:g.79478474G>A , CM000679.1:g.79478474G>A	GRCh37
NC_000017.9:g.77093069G>A	NCBI36
NG_011433.1:g.6354C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.542C>T	ENSP00000466346.2:p.Ala181Val
ENST00000571691.6:c.470C>T	ENSP00000461407.2:p.Ala157Val
ENST00000571721.6:c.542C>T	ENSP00000460660.2:p.Ala181Val
ENST00000572105.7:c.583C>T	ENSP00000462823.1:p.Leu195=
ENST00000573283.7:c.542C>T MANE Select	ENSP00000458435.1:p.Ala181Val
ENST00000574671.6:n.942C>T
ENST00000575659.6:c.542C>T	ENSP00000459119.2:p.Ala181Val
ENST00000575994.6:c.542C>T	ENSP00000460464.2:p.Ala181Val
ENST00000576214.3:n.843C>T
ENST00000576544.6:c.542C>T	ENSP00000461672.1:p.Ala181Val
ENST00000615544.5:c.542C>T	ENSP00000477968.1:p.Ala181Val
ENST00000644774.2:c.515C>T	ENSP00000493648.2:p.Ala172Val
ENST00000679410.1:n.666C>T
ENST00000679480.1:c.542C>T	ENSP00000506201.1:p.Ala181Val
ENST00000679535.1:n.843C>T
ENST00000679778.1:c.542C>T	ENSP00000505235.1:p.Ala181Val
ENST00000680227.1:c.542C>T	ENSP00000506253.1:p.Ala181Val
ENST00000680727.1:c.542C>T	ENSP00000505193.1:p.Ala181Val
ENST00000681052.1:c.542C>T	ENSP00000505060.1:p.Ala181Val
ENST00000681092.1:c.*346C>T	ENSP00000506720.1:n.*346C>T
ENST00000681842.1:c.542C>T	ENSP00000506126.1:p.Ala181Val
ENST00000331925.6:c.542C>T	ENSP00000331514.2:p.Ala181Val
ENST00000571691.5:c.515C>T	ENSP00000461407.1:p.Ala172Val
ENST00000572105.6:c.583C>T	ENSP00000462823.1:p.Leu195=
ENST00000573283.5:c.542C>T	ENSP00000458435.1:p.Ala181Val
ENST00000574671.5:n.401C>T
ENST00000575087.5:c.542C>T	ENSP00000459124.1:p.Ala181Val
ENST00000575659.5:c.542C>T	ENSP00000459119.1:p.Ala181Val
ENST00000575842.5:c.542C>T	ENSP00000458162.1:p.Ala181Val
ENST00000575994.5:c.542C>T	ENSP00000460464.1:p.Ala181Val
ENST00000576209.5:n.427C>T
ENST00000576214.2:n.740C>T
ENST00000576544.5:c.542C>T	ENSP00000461672.1:p.Ala181Val
ENST00000576917.5:n.595C>T
ENST00000615544.4:c.542C>T	ENSP00000477968.1:p.Ala181Val
NM_001199954.1:c.542C>T	NP_001186883.1:p.Ala181Val
NM_001614.3:c.542C>T	NP_001605.1:p.Ala181Val
NR_037688.1:n.681C>T
NM_001199954.2:c.542C>T	NP_001186883.1:p.Ala181Val
NM_001614.4:c.542C>T	NP_001605.1:p.Ala181Val
NR_037688.2:n.614C>T
NM_001614.5:c.542C>T MANE Select	NP_001605.1:p.Ala181Val
NR_037688.3:n.614C>T
NM_001199954.3:c.542C>T	NP_001186883.1:p.Ala181Val