Canonical Allele Identifier: CA2278540740

Gene: ACTG1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81512559_81512589delinsGGCCCCGCCCTGGACCCCCGGCGCCCCCCCA , CM000679.2:g.81512559_81512589delinsGGCCCCGCCCTGGACCCCCGGCGCCCCCCCA	GRCh38
NC_000017.10:g.79479585_79479615delinsGGCCCCGCCCTGGACCCCCGGCGCCCCCCCA , CM000679.1:g.79479585_79479615delinsGGCCCCGCCCTGGACCCCCGGCGCCCCCCCA	GRCh37
NC_000017.9:g.77094180_77094210delinsGGCCCCGCCCTGGACCCCCGGCGCCCCCCCA	NCBI36
NG_011433.1:g.5213_5243delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000466346.2:n.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGG...
ENST00000571691.6:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000461407.2:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000571721.6:c.-132_-102delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000460660.2:n.-132_-102delinsTGGGGGGGCGCCGGGGGTCCAGGGCG...
ENST00000572105.7:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000462823.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000573283.7:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC MANE Select	ENSP00000458435.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000574671.6:n.118+145_118+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC
ENST00000575659.6:c.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000459119.2:n.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000575994.6:c.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000460464.2:n.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000576214.3:n.118+145_118+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC
ENST00000576544.6:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000461672.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000615544.5:c.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000477968.1:n.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000644774.2:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000493648.2:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000679410.1:n.118+145_118+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC
ENST00000679480.1:c.-7+12_-7+42delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000506201.1:n.-7+12_-7+42delinsTGGGGGGGCGCCGGGGGTCCAGGG...
ENST00000679535.1:n.118+145_118+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC
ENST00000679778.1:c.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000505235.1:n.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000680227.1:c.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000506253.1:n.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGG...
ENST00000681052.1:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000505060.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000681092.1:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000506720.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000681842.1:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000506126.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000331925.6:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000331514.2:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000570382.1:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000466346.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000571691.5:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000461407.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000571721.5:c.-132_-102delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000460660.1:n.-132_-102delinsTGGGGGGGCGCCGGGGGTCCAGGGCG...
ENST00000572105.6:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000462823.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000573283.5:c.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000458435.1:n.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGG...
ENST00000575087.5:c.-7+17_-7+47delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000459124.1:n.-7+17_-7+47delinsTGGGGGGGCGCCGGGGGTCCAGGG...
ENST00000575659.5:c.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000459119.1:n.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000575842.5:c.-235_-205delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000458162.1:n.-235_-205delinsTGGGGGGGCGCCGGGGGTCCAGGGCG...
ENST00000575994.5:c.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000460464.1:n.-6-229_-6-199delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000576214.2:n.15+145_15+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC
ENST00000576544.5:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000461672.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
ENST00000576917.5:n.47+145_47+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC
ENST00000615544.4:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	ENSP00000477968.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAG...
NM_001199954.1:c.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	NP_001186883.1:n.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGGCGG...
NM_001614.3:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	NP_001605.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGG...
NR_037688.1:n.133+145_133+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC
NM_001199954.2:c.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	NP_001186883.1:n.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGGCGG...
NM_001614.4:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	NP_001605.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGG...
NR_037688.2:n.66+145_66+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC
NM_001614.5:c.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC MANE Select	NP_001605.1:n.-7+145_-7+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGG...
NR_037688.3:n.66+145_66+175delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC
NM_001199954.3:c.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGGCGGGGCC	NP_001186883.1:n.-7+26_-7+56delinsTGGGGGGGCGCCGGGGGTCCAGGGCGG...