Canonical Allele Identifier: CA2640434593
Gene: ACTG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81511123_81511128del , CM000679.2:g.81511123_81511128del GRCh38
NC_000017.10:g.79478149_79478154del , CM000679.1:g.79478149_79478154del GRCh37
NC_000017.9:g.77092744_77092749del NCBI36
NG_011433.1:g.6675_6680del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570382.2:c.803-19_803-14del ENSP00000466346.2:n.803-19_803-14del
ENST00000571691.6:c.731-19_731-14del ENSP00000461407.2:n.731-19_731-14del
ENST00000571721.6:c.803-19_803-14del ENSP00000460660.2:n.803-19_803-14del
ENST00000572105.7:c.*247-19_*247-14del ENSP00000462823.1:n.*247-19_*247-14del
ENST00000573283.7:c.803-19_803-14del MANE Select ENSP00000458435.1:n.803-19_803-14del
ENST00000574671.6:n.1203-19_1203-14del
ENST00000575659.6:c.803-19_803-14del ENSP00000459119.2:n.803-19_803-14del
ENST00000575994.6:c.803-19_803-14del ENSP00000460464.2:n.803-19_803-14del
ENST00000576214.3:n.1104-19_1104-14del
ENST00000576544.6:c.803-19_803-14del ENSP00000461672.1:n.803-19_803-14del
ENST00000615544.5:c.803-19_803-14del ENSP00000477968.1:n.803-19_803-14del
ENST00000644774.2:c.776-19_776-14del ENSP00000493648.2:n.776-19_776-14del
ENST00000679410.1:n.987_992del
ENST00000679480.1:c.803-19_803-14del ENSP00000506201.1:n.803-19_803-14del
ENST00000679535.1:n.1104-19_1104-14del
ENST00000679778.1:c.803-19_803-14del ENSP00000505235.1:n.803-19_803-14del
ENST00000680227.1:c.803-19_803-14del ENSP00000506253.1:n.803-19_803-14del
ENST00000680727.1:c.803-19_803-14del ENSP00000505193.1:n.803-19_803-14del
ENST00000681052.1:c.803-19_803-14del ENSP00000505060.1:n.803-19_803-14del
ENST00000681092.1:c.*607-19_*607-14del ENSP00000506720.1:n.*607-19_*607-14del
ENST00000681842.1:c.803-19_803-14del ENSP00000506126.1:n.803-19_803-14del
ENST00000331925.6:c.803-19_803-14del ENSP00000331514.2:n.803-19_803-14del
ENST00000572105.6:c.*247-19_*247-14del ENSP00000462823.1:n.*247-19_*247-14del
ENST00000573283.5:c.803-19_803-14del ENSP00000458435.1:n.803-19_803-14del
ENST00000574671.5:n.662-19_662-14del
ENST00000575087.5:c.803-19_803-14del ENSP00000459124.1:n.803-19_803-14del
ENST00000575842.5:c.803-19_803-14del ENSP00000458162.1:n.803-19_803-14del
ENST00000576209.5:n.688-19_688-14del
ENST00000576214.2:n.1001-19_1001-14del
ENST00000576544.5:c.803-19_803-14del ENSP00000461672.1:n.803-19_803-14del
ENST00000576917.5:n.916_921del
ENST00000615544.4:c.803-19_803-14del ENSP00000477968.1:n.803-19_803-14del
NM_001199954.1:c.803-19_803-14del NP_001186883.1:n.803-19_803-14del
NM_001614.3:c.803-19_803-14del NP_001605.1:n.803-19_803-14del
NR_037688.1:n.942-19_942-14del
NM_001199954.2:c.803-19_803-14del NP_001186883.1:n.803-19_803-14del
NM_001614.4:c.803-19_803-14del NP_001605.1:n.803-19_803-14del
NR_037688.2:n.875-19_875-14del
NM_001614.5:c.803-19_803-14del MANE Select NP_001605.1:n.803-19_803-14del
NR_037688.3:n.875-19_875-14del
NM_001199954.3:c.803-19_803-14del NP_001186883.1:n.803-19_803-14del