Canonical Allele Identifier: CA295069849
Gene: ACTG1 HGNC NCBI

Linked Data

dbSNP Id: rs1016880511
MyVariant Identifiers: chr17:g.81512654G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81512654G>A , CM000679.2:g.81512654G>A GRCh38
NC_000017.10:g.79479680G>A , CM000679.1:g.79479680G>A GRCh37
NC_000017.9:g.77094275G>A NCBI36
NG_011433.1:g.5148C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000570382.2:c.-46C>T ENSP00000466346.2:n.-46C>T
ENST00000571691.6:c.-7+80C>T ENSP00000461407.2:n.-7+80C>T
ENST00000571721.6:c.-197C>T ENSP00000460660.2:n.-197C>T
ENST00000572105.7:c.-7+80C>T ENSP00000462823.1:n.-7+80C>T
ENST00000573283.7:c.-7+80C>T MANE Select ENSP00000458435.1:n.-7+80C>T
ENST00000574671.6:n.118+80C>T
ENST00000575659.6:c.-6-294C>T ENSP00000459119.2:n.-6-294C>T
ENST00000575994.6:c.-6-294C>T ENSP00000460464.2:n.-6-294C>T
ENST00000576214.3:n.118+80C>T
ENST00000576544.6:c.-7+80C>T ENSP00000461672.1:n.-7+80C>T
ENST00000615544.5:c.-6-294C>T ENSP00000477968.1:n.-6-294C>T
ENST00000644774.2:c.-7+80C>T ENSP00000493648.2:n.-7+80C>T
ENST00000679410.1:n.118+80C>T
ENST00000679480.1:c.-60C>T ENSP00000506201.1:n.-60C>T
ENST00000679535.1:n.118+80C>T
ENST00000679778.1:c.-6-294C>T ENSP00000505235.1:n.-6-294C>T
ENST00000680227.1:c.-46C>T ENSP00000506253.1:n.-46C>T
ENST00000681052.1:c.-7+80C>T ENSP00000505060.1:n.-7+80C>T
ENST00000681092.1:c.-7+80C>T ENSP00000506720.1:n.-7+80C>T
ENST00000681842.1:c.-7+80C>T ENSP00000506126.1:n.-7+80C>T
ENST00000331925.6:c.-7+80C>T ENSP00000331514.2:n.-7+80C>T
ENST00000570382.1:c.-7+80C>T ENSP00000466346.1:n.-7+80C>T
ENST00000571691.5:c.-7+80C>T ENSP00000461407.1:n.-7+80C>T
ENST00000571721.5:c.-197C>T ENSP00000460660.1:n.-197C>T
ENST00000572105.6:c.-7+80C>T ENSP00000462823.1:n.-7+80C>T
ENST00000573283.5:c.-46C>T ENSP00000458435.1:n.-46C>T
ENST00000575087.5:c.-55C>T ENSP00000459124.1:n.-55C>T
ENST00000575659.5:c.-6-294C>T ENSP00000459119.1:n.-6-294C>T
ENST00000575842.5:c.-300C>T ENSP00000458162.1:n.-300C>T
ENST00000575994.5:c.-6-294C>T ENSP00000460464.1:n.-6-294C>T
ENST00000576214.2:n.15+80C>T
ENST00000576544.5:c.-7+80C>T ENSP00000461672.1:n.-7+80C>T
ENST00000576917.5:n.47+80C>T
ENST00000615544.4:c.-7+80C>T ENSP00000477968.1:n.-7+80C>T
NM_001199954.1:c.-46C>T NP_001186883.1:n.-46C>T
NM_001614.3:c.-7+80C>T NP_001605.1:n.-7+80C>T
NR_037688.1:n.133+80C>T
NM_001199954.2:c.-46C>T NP_001186883.1:n.-46C>T
NM_001614.4:c.-7+80C>T NP_001605.1:n.-7+80C>T
NR_037688.2:n.66+80C>T
NM_001614.5:c.-7+80C>T MANE Select NP_001605.1:n.-7+80C>T
NR_037688.3:n.66+80C>T
NM_001199954.3:c.-46C>T NP_001186883.1:n.-46C>T