Canonical Allele Identifier: CA2278541029

Gene: ACTG1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81512800A= , CM000679.2:g.81512800A=	GRCh38
NC_000017.10:g.79479826A= , CM000679.1:g.79479826A=	GRCh37
NC_000017.9:g.77094421A=	NCBI36
NG_011433.1:g.5002T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.-192T=	ENSP00000466346.2:n.-192T=
ENST00000572105.7:c.-73T=	ENSP00000462823.1:n.-73T=
ENST00000574671.6:n.52T=
ENST00000575659.6:c.-6-440T=	ENSP00000459119.2:n.-6-440T=
ENST00000575994.6:c.-6-440T=	ENSP00000460464.2:n.-6-440T=
ENST00000576214.3:n.52T=
ENST00000576544.6:c.-73T=	ENSP00000461672.1:n.-73T=
ENST00000615544.5:c.-6-440T=	ENSP00000477968.1:n.-6-440T=
ENST00000679410.1:n.52T=
ENST00000679535.1:n.52T=
ENST00000679778.1:c.-6-440T=	ENSP00000505235.1:n.-6-440T=
ENST00000681052.1:c.-67-6T=	ENSP00000505060.1:n.-67-6T=
ENST00000681092.1:c.-73T=	ENSP00000506720.1:n.-73T=
ENST00000681842.1:c.-73T=	ENSP00000506126.1:n.-73T=
ENST00000331925.6:c.-73T=	ENSP00000331514.2:n.-73T=
ENST00000575659.5:c.-6-440T=	ENSP00000459119.1:n.-6-440T=
ENST00000575994.5:c.-6-440T=	ENSP00000460464.1:n.-6-440T=
NM_001199954.1:c.-192T=	NP_001186883.1:n.-192T=
NM_001614.3:c.-73T=	NP_001605.1:n.-73T=
NR_037688.1:n.67T=