Canonical Allele Identifier: CA2278540766

Gene: ACTG1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81512581_81512582delinsGC , CM000679.2:g.81512581_81512582delinsGC	GRCh38
NC_000017.10:g.79479607_79479608delinsGC , CM000679.1:g.79479607_79479608delinsGC	GRCh37
NC_000017.9:g.77094202_77094203delinsGC	NCBI36
NG_011433.1:g.5220_5221delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.-7+33_-7+34delinsGC	ENSP00000466346.2:n.-7+33_-7+34delinsGC
ENST00000571691.6:c.-7+152_-7+153delinsGC	ENSP00000461407.2:n.-7+152_-7+153delinsGC
ENST00000571721.6:c.-125_-124delinsGC	ENSP00000460660.2:n.-125_-124delinsGC
ENST00000572105.7:c.-7+152_-7+153delinsGC	ENSP00000462823.1:n.-7+152_-7+153delinsGC
ENST00000573283.7:c.-7+152_-7+153delinsGC MANE Select	ENSP00000458435.1:n.-7+152_-7+153delinsGC
ENST00000574671.6:n.118+152_118+153delinsGC
ENST00000575659.6:c.-6-222_-6-221delinsGC	ENSP00000459119.2:n.-6-222_-6-221delinsGC
ENST00000575994.6:c.-6-222_-6-221delinsGC	ENSP00000460464.2:n.-6-222_-6-221delinsGC
ENST00000576214.3:n.118+152_118+153delinsGC
ENST00000576544.6:c.-7+152_-7+153delinsGC	ENSP00000461672.1:n.-7+152_-7+153delinsGC
ENST00000615544.5:c.-6-222_-6-221delinsGC	ENSP00000477968.1:n.-6-222_-6-221delinsGC
ENST00000644774.2:c.-7+152_-7+153delinsGC	ENSP00000493648.2:n.-7+152_-7+153delinsGC
ENST00000679410.1:n.118+152_118+153delinsGC
ENST00000679480.1:c.-7+19_-7+20delinsGC	ENSP00000506201.1:n.-7+19_-7+20delinsGC
ENST00000679535.1:n.118+152_118+153delinsGC
ENST00000679778.1:c.-6-222_-6-221delinsGC	ENSP00000505235.1:n.-6-222_-6-221delinsGC
ENST00000680227.1:c.-7+33_-7+34delinsGC	ENSP00000506253.1:n.-7+33_-7+34delinsGC
ENST00000681052.1:c.-7+152_-7+153delinsGC	ENSP00000505060.1:n.-7+152_-7+153delinsGC
ENST00000681092.1:c.-7+152_-7+153delinsGC	ENSP00000506720.1:n.-7+152_-7+153delinsGC
ENST00000681842.1:c.-7+152_-7+153delinsGC	ENSP00000506126.1:n.-7+152_-7+153delinsGC
ENST00000331925.6:c.-7+152_-7+153delinsGC	ENSP00000331514.2:n.-7+152_-7+153delinsGC
ENST00000570382.1:c.-7+152_-7+153delinsGC	ENSP00000466346.1:n.-7+152_-7+153delinsGC
ENST00000571691.5:c.-7+152_-7+153delinsGC	ENSP00000461407.1:n.-7+152_-7+153delinsGC
ENST00000571721.5:c.-125_-124delinsGC	ENSP00000460660.1:n.-125_-124delinsGC
ENST00000572105.6:c.-7+152_-7+153delinsGC	ENSP00000462823.1:n.-7+152_-7+153delinsGC
ENST00000573283.5:c.-7+33_-7+34delinsGC	ENSP00000458435.1:n.-7+33_-7+34delinsGC
ENST00000575087.5:c.-7+24_-7+25delinsGC	ENSP00000459124.1:n.-7+24_-7+25delinsGC
ENST00000575659.5:c.-6-222_-6-221delinsGC	ENSP00000459119.1:n.-6-222_-6-221delinsGC
ENST00000575842.5:c.-228_-227delinsGC	ENSP00000458162.1:n.-228_-227delinsGC
ENST00000575994.5:c.-6-222_-6-221delinsGC	ENSP00000460464.1:n.-6-222_-6-221delinsGC
ENST00000576214.2:n.15+152_15+153delinsGC
ENST00000576544.5:c.-7+152_-7+153delinsGC	ENSP00000461672.1:n.-7+152_-7+153delinsGC
ENST00000576917.5:n.47+152_47+153delinsGC
ENST00000615544.4:c.-7+152_-7+153delinsGC	ENSP00000477968.1:n.-7+152_-7+153delinsGC
NM_001199954.1:c.-7+33_-7+34delinsGC	NP_001186883.1:n.-7+33_-7+34delinsGC
NM_001614.3:c.-7+152_-7+153delinsGC	NP_001605.1:n.-7+152_-7+153delinsGC
NR_037688.1:n.133+152_133+153delinsGC
NM_001199954.2:c.-7+33_-7+34delinsGC	NP_001186883.1:n.-7+33_-7+34delinsGC
NM_001614.4:c.-7+152_-7+153delinsGC	NP_001605.1:n.-7+152_-7+153delinsGC
NR_037688.2:n.66+152_66+153delinsGC
NM_001614.5:c.-7+152_-7+153delinsGC MANE Select	NP_001605.1:n.-7+152_-7+153delinsGC
NR_037688.3:n.66+152_66+153delinsGC
NM_001199954.3:c.-7+33_-7+34delinsGC	NP_001186883.1:n.-7+33_-7+34delinsGC