Canonical Allele Identifier: CA2278540986
Gene: ACTG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81512764A= , CM000679.2:g.81512764A= GRCh38
NC_000017.10:g.79479790A= , CM000679.1:g.79479790A= GRCh37
NC_000017.9:g.77094385A= NCBI36
NG_011433.1:g.5038T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000570382.2:c.-156T= ENSP00000466346.2:n.-156T=
ENST00000571691.6:c.-37T= ENSP00000461407.2:n.-37T=
ENST00000571721.6:c.-307T= ENSP00000460660.2:n.-307T=
ENST00000572105.7:c.-37T= ENSP00000462823.1:n.-37T=
ENST00000573283.7:c.-37T= MANE Select ENSP00000458435.1:n.-37T=
ENST00000574671.6:n.88T=
ENST00000575659.6:c.-6-404T= ENSP00000459119.2:n.-6-404T=
ENST00000575994.6:c.-6-404T= ENSP00000460464.2:n.-6-404T=
ENST00000576214.3:n.88T=
ENST00000576544.6:c.-37T= ENSP00000461672.1:n.-37T=
ENST00000615544.5:c.-6-404T= ENSP00000477968.1:n.-6-404T=
ENST00000679410.1:n.88T=
ENST00000679535.1:n.88T=
ENST00000679778.1:c.-6-404T= ENSP00000505235.1:n.-6-404T=
ENST00000680227.1:c.-156T= ENSP00000506253.1:n.-156T=
ENST00000681052.1:c.-37T= ENSP00000505060.1:n.-37T=
ENST00000681092.1:c.-37T= ENSP00000506720.1:n.-37T=
ENST00000681842.1:c.-37T= ENSP00000506126.1:n.-37T=
ENST00000331925.6:c.-37T= ENSP00000331514.2:n.-37T=
ENST00000570382.1:c.-37T= ENSP00000466346.1:n.-37T=
ENST00000571721.5:c.-307T= ENSP00000460660.1:n.-307T=
ENST00000572105.6:c.-37T= ENSP00000462823.1:n.-37T=
ENST00000573283.5:c.-156T= ENSP00000458435.1:n.-156T=
ENST00000575087.5:c.-165T= ENSP00000459124.1:n.-165T=
ENST00000575659.5:c.-6-404T= ENSP00000459119.1:n.-6-404T=
ENST00000575842.5:c.-410T= ENSP00000458162.1:n.-410T=
ENST00000575994.5:c.-6-404T= ENSP00000460464.1:n.-6-404T=
ENST00000576544.5:c.-37T= ENSP00000461672.1:n.-37T=
ENST00000576917.5:n.17T=
NM_001199954.1:c.-156T= NP_001186883.1:n.-156T=
NM_001614.3:c.-37T= NP_001605.1:n.-37T=
NR_037688.1:n.103T=
NM_001199954.2:c.-156T= NP_001186883.1:n.-156T=
NM_001614.4:c.-37T= NP_001605.1:n.-37T=
NR_037688.2:n.36T=
NM_001614.5:c.-37T= MANE Select NP_001605.1:n.-37T=
NR_037688.3:n.36T=
NM_001199954.3:c.-156T= NP_001186883.1:n.-156T=