Canonical Allele Identifier: CA2810629653
Gene: ACTG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81512757_81512764dup , CM000679.2:g.81512757_81512764dup GRCh38
NC_000017.10:g.79479783_79479790dup , CM000679.1:g.79479783_79479790dup GRCh37
NC_000017.9:g.77094378_77094385dup NCBI36
NG_011433.1:g.5045_5052dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000570382.2:c.-149_-142dup ENSP00000466346.2:n.-149_-142dup
ENST00000571691.6:c.-30_-23dup ENSP00000461407.2:n.-30_-23dup
ENST00000571721.6:c.-300_-293dup ENSP00000460660.2:n.-300_-293dup
ENST00000572105.7:c.-30_-23dup ENSP00000462823.1:n.-30_-23dup
ENST00000573283.7:c.-30_-23dup MANE Select ENSP00000458435.1:n.-30_-23dup
ENST00000574671.6:n.95_102dup
ENST00000575659.6:c.-6-397_-6-390dup ENSP00000459119.2:n.-6-397_-6-390dup
ENST00000575994.6:c.-6-397_-6-390dup ENSP00000460464.2:n.-6-397_-6-390dup
ENST00000576214.3:n.95_102dup
ENST00000576544.6:c.-30_-23dup ENSP00000461672.1:n.-30_-23dup
ENST00000615544.5:c.-6-397_-6-390dup ENSP00000477968.1:n.-6-397_-6-390dup
ENST00000679410.1:n.95_102dup
ENST00000679535.1:n.95_102dup
ENST00000679778.1:c.-6-397_-6-390dup ENSP00000505235.1:n.-6-397_-6-390dup
ENST00000680227.1:c.-149_-142dup ENSP00000506253.1:n.-149_-142dup
ENST00000681052.1:c.-30_-23dup ENSP00000505060.1:n.-30_-23dup
ENST00000681092.1:c.-30_-23dup ENSP00000506720.1:n.-30_-23dup
ENST00000681842.1:c.-30_-23dup ENSP00000506126.1:n.-30_-23dup
ENST00000331925.6:c.-30_-23dup ENSP00000331514.2:n.-30_-23dup
ENST00000570382.1:c.-30_-23dup ENSP00000466346.1:n.-30_-23dup
ENST00000571721.5:c.-300_-293dup ENSP00000460660.1:n.-300_-293dup
ENST00000572105.6:c.-30_-23dup ENSP00000462823.1:n.-30_-23dup
ENST00000573283.5:c.-149_-142dup ENSP00000458435.1:n.-149_-142dup
ENST00000575087.5:c.-158_-151dup ENSP00000459124.1:n.-158_-151dup
ENST00000575659.5:c.-6-397_-6-390dup ENSP00000459119.1:n.-6-397_-6-390dup
ENST00000575842.5:c.-403_-396dup ENSP00000458162.1:n.-403_-396dup
ENST00000575994.5:c.-6-397_-6-390dup ENSP00000460464.1:n.-6-397_-6-390dup
ENST00000576544.5:c.-30_-23dup ENSP00000461672.1:n.-30_-23dup
ENST00000576917.5:n.24_31dup
NM_001199954.1:c.-149_-142dup NP_001186883.1:n.-149_-142dup
NM_001614.3:c.-30_-23dup NP_001605.1:n.-30_-23dup
NR_037688.1:n.110_117dup
NM_001199954.2:c.-149_-142dup NP_001186883.1:n.-149_-142dup
NM_001614.4:c.-30_-23dup NP_001605.1:n.-30_-23dup
NR_037688.2:n.43_50dup
NM_001614.5:c.-30_-23dup MANE Select NP_001605.1:n.-30_-23dup
NR_037688.3:n.43_50dup
NM_001199954.3:c.-149_-142dup NP_001186883.1:n.-149_-142dup