Canonical Allele Identifier: CA2278541003

Gene: ACTG1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81512779G= , CM000679.2:g.81512779G=	GRCh38
NC_000017.10:g.79479805G= , CM000679.1:g.79479805G=	GRCh37
NC_000017.9:g.77094400G=	NCBI36
NG_011433.1:g.5023C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.-171C=	ENSP00000466346.2:n.-171C=
ENST00000571691.6:c.-52C=	ENSP00000461407.2:n.-52C=
ENST00000572105.7:c.-52C=	ENSP00000462823.1:n.-52C=
ENST00000573283.7:c.-52C= MANE Select	ENSP00000458435.1:n.-52C=
ENST00000574671.6:n.73C=
ENST00000575659.6:c.-6-419C=	ENSP00000459119.2:n.-6-419C=
ENST00000575994.6:c.-6-419C=	ENSP00000460464.2:n.-6-419C=
ENST00000576214.3:n.73C=
ENST00000576544.6:c.-52C=	ENSP00000461672.1:n.-52C=
ENST00000615544.5:c.-6-419C=	ENSP00000477968.1:n.-6-419C=
ENST00000679410.1:n.73C=
ENST00000679535.1:n.73C=
ENST00000679778.1:c.-6-419C=	ENSP00000505235.1:n.-6-419C=
ENST00000681052.1:c.-52C=	ENSP00000505060.1:n.-52C=
ENST00000681092.1:c.-52C=	ENSP00000506720.1:n.-52C=
ENST00000681842.1:c.-52C=	ENSP00000506126.1:n.-52C=
ENST00000331925.6:c.-52C=	ENSP00000331514.2:n.-52C=
ENST00000570382.1:c.-52C=	ENSP00000466346.1:n.-52C=
ENST00000572105.6:c.-52C=	ENSP00000462823.1:n.-52C=
ENST00000573283.5:c.-171C=	ENSP00000458435.1:n.-171C=
ENST00000575087.5:c.-180C=	ENSP00000459124.1:n.-180C=
ENST00000575659.5:c.-6-419C=	ENSP00000459119.1:n.-6-419C=
ENST00000575842.5:c.-425C=	ENSP00000458162.1:n.-425C=
ENST00000575994.5:c.-6-419C=	ENSP00000460464.1:n.-6-419C=
ENST00000576544.5:c.-52C=	ENSP00000461672.1:n.-52C=
ENST00000576917.5:n.2C=
NM_001199954.1:c.-171C=	NP_001186883.1:n.-171C=
NM_001614.3:c.-52C=	NP_001605.1:n.-52C=
NR_037688.1:n.88C=
NM_001199954.2:c.-171C=	NP_001186883.1:n.-171C=
NM_001614.4:c.-52C=	NP_001605.1:n.-52C=
NR_037688.2:n.21C=
NM_001614.5:c.-52C= MANE Select	NP_001605.1:n.-52C=
NR_037688.3:n.21C=
NM_001199954.3:c.-171C=	NP_001186883.1:n.-171C=