Canonical Allele Identifier: CA2599063476
Gene: ACTG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81512728_81512733del , CM000679.2:g.81512728_81512733del GRCh38
NC_000017.10:g.79479754_79479759del , CM000679.1:g.79479754_79479759del GRCh37
NC_000017.9:g.77094349_77094354del NCBI36
NG_011433.1:g.5070_5075del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570382.2:c.-124_-119del ENSP00000466346.2:n.-124_-119del
ENST00000571691.6:c.-7+2_-7+7del ENSP00000461407.2:n.-7+2_-7+7del
ENST00000571721.6:c.-275_-270del ENSP00000460660.2:n.-275_-270del
ENST00000572105.7:c.-7+2_-7+7del ENSP00000462823.1:n.-7+2_-7+7del
ENST00000573283.7:c.-7+2_-7+7del MANE Select ENSP00000458435.1:n.-7+2_-7+7del
ENST00000574671.6:n.118+2_118+7del
ENST00000575659.6:c.-6-372_-6-367del ENSP00000459119.2:n.-6-372_-6-367del
ENST00000575994.6:c.-6-372_-6-367del ENSP00000460464.2:n.-6-372_-6-367del
ENST00000576214.3:n.118+2_118+7del
ENST00000576544.6:c.-7+2_-7+7del ENSP00000461672.1:n.-7+2_-7+7del
ENST00000615544.5:c.-6-372_-6-367del ENSP00000477968.1:n.-6-372_-6-367del
ENST00000644774.2:c.-7+2_-7+7del ENSP00000493648.2:n.-7+2_-7+7del
ENST00000679410.1:n.118+2_118+7del
ENST00000679535.1:n.118+2_118+7del
ENST00000679778.1:c.-6-372_-6-367del ENSP00000505235.1:n.-6-372_-6-367del
ENST00000680227.1:c.-124_-119del ENSP00000506253.1:n.-124_-119del
ENST00000681052.1:c.-7+2_-7+7del ENSP00000505060.1:n.-7+2_-7+7del
ENST00000681092.1:c.-7+2_-7+7del ENSP00000506720.1:n.-7+2_-7+7del
ENST00000681842.1:c.-7+2_-7+7del ENSP00000506126.1:n.-7+2_-7+7del
ENST00000331925.6:c.-7+2_-7+7del ENSP00000331514.2:n.-7+2_-7+7del
ENST00000570382.1:c.-7+2_-7+7del ENSP00000466346.1:n.-7+2_-7+7del
ENST00000571691.5:c.-7+2_-7+7del ENSP00000461407.1:n.-7+2_-7+7del
ENST00000571721.5:c.-275_-270del ENSP00000460660.1:n.-275_-270del
ENST00000572105.6:c.-7+2_-7+7del ENSP00000462823.1:n.-7+2_-7+7del
ENST00000573283.5:c.-124_-119del ENSP00000458435.1:n.-124_-119del
ENST00000575087.5:c.-133_-128del ENSP00000459124.1:n.-133_-128del
ENST00000575659.5:c.-6-372_-6-367del ENSP00000459119.1:n.-6-372_-6-367del
ENST00000575842.5:c.-378_-373del ENSP00000458162.1:n.-378_-373del
ENST00000575994.5:c.-6-372_-6-367del ENSP00000460464.1:n.-6-372_-6-367del
ENST00000576214.2:n.15+2_15+7del
ENST00000576544.5:c.-7+2_-7+7del ENSP00000461672.1:n.-7+2_-7+7del
ENST00000576917.5:n.47+2_47+7del
ENST00000615544.4:c.-7+2_-7+7del ENSP00000477968.1:n.-7+2_-7+7del
NM_001199954.1:c.-124_-119del NP_001186883.1:n.-124_-119del
NM_001614.3:c.-7+2_-7+7del NP_001605.1:n.-7+2_-7+7del
NR_037688.1:n.133+2_133+7del
NM_001199954.2:c.-124_-119del NP_001186883.1:n.-124_-119del
NM_001614.4:c.-7+2_-7+7del NP_001605.1:n.-7+2_-7+7del
NR_037688.2:n.66+2_66+7del
NM_001614.5:c.-7+2_-7+7del MANE Select NP_001605.1:n.-7+2_-7+7del
NR_037688.3:n.66+2_66+7del
NM_001199954.3:c.-124_-119del NP_001186883.1:n.-124_-119del