Canonical Allele Identifier: CA2278539833

Gene: ACTG1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511490T= , CM000679.2:g.81511490T=	GRCh38
NC_000017.10:g.79478516T= , CM000679.1:g.79478516T=	GRCh37
NC_000017.9:g.77093111T=	NCBI36
NG_011433.1:g.6312A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.500A=	ENSP00000466346.2:p.Glu167=
ENST00000571691.6:c.428A=	ENSP00000461407.2:p.Glu143=
ENST00000571721.6:c.500A=	ENSP00000460660.2:p.Glu167=
ENST00000572105.7:c.541A=	ENSP00000462823.1:p.Arg181=
ENST00000573283.7:c.500A= MANE Select	ENSP00000458435.1:p.Glu167=
ENST00000574671.6:n.900A=
ENST00000575659.6:c.500A=	ENSP00000459119.2:p.Glu167=
ENST00000575994.6:c.500A=	ENSP00000460464.2:p.Glu167=
ENST00000576214.3:n.801A=
ENST00000576544.6:c.500A=	ENSP00000461672.1:p.Glu167=
ENST00000615544.5:c.500A=	ENSP00000477968.1:p.Glu167=
ENST00000644774.2:c.473A=	ENSP00000493648.2:p.Glu158=
ENST00000679410.1:n.624A=
ENST00000679480.1:c.500A=	ENSP00000506201.1:p.Glu167=
ENST00000679535.1:n.801A=
ENST00000679778.1:c.500A=	ENSP00000505235.1:p.Glu167=
ENST00000680227.1:c.500A=	ENSP00000506253.1:p.Glu167=
ENST00000680727.1:c.500A=	ENSP00000505193.1:p.Glu167=
ENST00000681052.1:c.500A=	ENSP00000505060.1:p.Glu167=
ENST00000681092.1:c.*304A=	ENSP00000506720.1:n.*304A=
ENST00000681842.1:c.500A=	ENSP00000506126.1:p.Glu167=
ENST00000331925.6:c.500A=	ENSP00000331514.2:p.Glu167=
ENST00000571691.5:c.473A=	ENSP00000461407.1:p.Glu158=
ENST00000572105.6:c.541A=	ENSP00000462823.1:p.Arg181=
ENST00000573283.5:c.500A=	ENSP00000458435.1:p.Glu167=
ENST00000574671.5:n.359A=
ENST00000575087.5:c.500A=	ENSP00000459124.1:p.Glu167=
ENST00000575659.5:c.500A=	ENSP00000459119.1:p.Glu167=
ENST00000575842.5:c.500A=	ENSP00000458162.1:p.Glu167=
ENST00000575994.5:c.500A=	ENSP00000460464.1:p.Glu167=
ENST00000576209.5:n.385A=
ENST00000576214.2:n.698A=
ENST00000576544.5:c.500A=	ENSP00000461672.1:p.Glu167=
ENST00000576917.5:n.553A=
ENST00000615544.4:c.500A=	ENSP00000477968.1:p.Glu167=
NM_001199954.1:c.500A=	NP_001186883.1:p.Glu167=
NM_001614.3:c.500A=	NP_001605.1:p.Glu167=
NR_037688.1:n.639A=
NM_001199954.2:c.500A=	NP_001186883.1:p.Glu167=
NM_001614.4:c.500A=	NP_001605.1:p.Glu167=
NR_037688.2:n.572A=
NM_001614.5:c.500A= MANE Select	NP_001605.1:p.Glu167=
NR_037688.3:n.572A=
NM_001199954.3:c.500A=	NP_001186883.1:p.Glu167=