Canonical Allele Identifier: CA2553238493

Gene: ACTG1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511176_81511177insT , CM000679.2:g.81511176_81511177insT	GRCh38
NC_000017.10:g.79478202_79478203insT , CM000679.1:g.79478202_79478203insT	GRCh37
NC_000017.9:g.77092797_77092798insT	NCBI36
NG_011433.1:g.6625_6626insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.802+11_802+12insA	ENSP00000466346.2:n.802+11_802+12insA
ENST00000571691.6:c.730+11_730+12insA	ENSP00000461407.2:n.730+11_730+12insA
ENST00000571721.6:c.802+11_802+12insA	ENSP00000460660.2:n.802+11_802+12insA
ENST00000572105.7:c.*246+11_*246+12insA	ENSP00000462823.1:n.*246+11_*246+12insA
ENST00000573283.7:c.802+11_802+12insA MANE Select	ENSP00000458435.1:n.802+11_802+12insA
ENST00000574671.6:n.1202+11_1202+12insA
ENST00000575659.6:c.802+11_802+12insA	ENSP00000459119.2:n.802+11_802+12insA
ENST00000575994.6:c.802+11_802+12insA	ENSP00000460464.2:n.802+11_802+12insA
ENST00000576214.3:n.1103+11_1103+12insA
ENST00000576544.6:c.802+11_802+12insA	ENSP00000461672.1:n.802+11_802+12insA
ENST00000615544.5:c.802+11_802+12insA	ENSP00000477968.1:n.802+11_802+12insA
ENST00000644774.2:c.775+11_775+12insA	ENSP00000493648.2:n.775+11_775+12insA
ENST00000679410.1:n.937_938insA
ENST00000679480.1:c.802+11_802+12insA	ENSP00000506201.1:n.802+11_802+12insA
ENST00000679535.1:n.1103+11_1103+12insA
ENST00000679778.1:c.802+11_802+12insA	ENSP00000505235.1:n.802+11_802+12insA
ENST00000680227.1:c.802+11_802+12insA	ENSP00000506253.1:n.802+11_802+12insA
ENST00000680727.1:c.802+11_802+12insA	ENSP00000505193.1:n.802+11_802+12insA
ENST00000681052.1:c.802+11_802+12insA	ENSP00000505060.1:n.802+11_802+12insA
ENST00000681092.1:c.*606+11_*606+12insA	ENSP00000506720.1:n.*606+11_*606+12insA
ENST00000681842.1:c.802+11_802+12insA	ENSP00000506126.1:n.802+11_802+12insA
ENST00000331925.6:c.802+11_802+12insA	ENSP00000331514.2:n.802+11_802+12insA
ENST00000572105.6:c.*246+11_*246+12insA	ENSP00000462823.1:n.*246+11_*246+12insA
ENST00000573283.5:c.802+11_802+12insA	ENSP00000458435.1:n.802+11_802+12insA
ENST00000574671.5:n.661+11_661+12insA
ENST00000575087.5:c.802+11_802+12insA	ENSP00000459124.1:n.802+11_802+12insA
ENST00000575842.5:c.802+11_802+12insA	ENSP00000458162.1:n.802+11_802+12insA
ENST00000576209.5:n.687+11_687+12insA
ENST00000576214.2:n.1000+11_1000+12insA
ENST00000576544.5:c.802+11_802+12insA	ENSP00000461672.1:n.802+11_802+12insA
ENST00000576917.5:n.866_867insA
ENST00000615544.4:c.802+11_802+12insA	ENSP00000477968.1:n.802+11_802+12insA
NM_001199954.1:c.802+11_802+12insA	NP_001186883.1:n.802+11_802+12insA
NM_001614.3:c.802+11_802+12insA	NP_001605.1:n.802+11_802+12insA
NR_037688.1:n.941+11_941+12insA
NM_001199954.2:c.802+11_802+12insA	NP_001186883.1:n.802+11_802+12insA
NM_001614.4:c.802+11_802+12insA	NP_001605.1:n.802+11_802+12insA
NR_037688.2:n.874+11_874+12insA
NM_001614.5:c.802+11_802+12insA MANE Select	NP_001605.1:n.802+11_802+12insA
NR_037688.3:n.874+11_874+12insA
NM_001199954.3:c.802+11_802+12insA	NP_001186883.1:n.802+11_802+12insA