Canonical Allele Identifier: CA628022583

Gene: ACTG1

Linked Data

• dbSNP Id: rs200552253
• gnomAD v2: 17-79478662-G-C
• gnomAD v4: 17-81511636-G-C
• MyVariant Identifiers: chr17:g.79478662G>C (hg19) ; chr17:g.81511636G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511636G>C , CM000679.2:g.81511636G>C	GRCh38
NC_000017.10:g.79478662G>C , CM000679.1:g.79478662G>C	GRCh37
NC_000017.9:g.77093257G>C	NCBI36
NG_011433.1:g.6166C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000570382.2:c.364-10C>G	ENSP00000466346.2:n.364-10C>G
ENST00000571691.6:c.340-58C>G	ENSP00000461407.2:n.340-58C>G
ENST00000571721.6:c.364-10C>G	ENSP00000460660.2:n.364-10C>G
ENST00000572105.7:c.405-10C>G	ENSP00000462823.1:n.405-10C>G
ENST00000573283.7:c.364-10C>G MANE Select	ENSP00000458435.1:n.364-10C>G
ENST00000574671.6:n.754C>G
ENST00000575659.6:c.364-10C>G	ENSP00000459119.2:n.364-10C>G
ENST00000575994.6:c.364-10C>G	ENSP00000460464.2:n.364-10C>G
ENST00000576214.3:n.655C>G
ENST00000576544.6:c.364-10C>G	ENSP00000461672.1:n.364-10C>G
ENST00000615544.5:c.364-10C>G	ENSP00000477968.1:n.364-10C>G
ENST00000644774.2:c.337-10C>G	ENSP00000493648.2:n.337-10C>G
ENST00000679410.1:n.488-10C>G
ENST00000679480.1:c.364-10C>G	ENSP00000506201.1:n.364-10C>G
ENST00000679535.1:n.655C>G
ENST00000679778.1:c.364-10C>G	ENSP00000505235.1:n.364-10C>G
ENST00000680227.1:c.364-10C>G	ENSP00000506253.1:n.364-10C>G
ENST00000680727.1:c.364-10C>G	ENSP00000505193.1:n.364-10C>G
ENST00000681052.1:c.364-10C>G	ENSP00000505060.1:n.364-10C>G
ENST00000681092.1:c.*168-10C>G	ENSP00000506720.1:n.*168-10C>G
ENST00000681842.1:c.364-10C>G	ENSP00000506126.1:n.364-10C>G
ENST00000331925.6:c.364-10C>G	ENSP00000331514.2:n.364-10C>G
ENST00000570382.1:c.340-58C>G	ENSP00000466346.1:n.340-58C>G
ENST00000571691.5:c.337-10C>G	ENSP00000461407.1:n.337-10C>G
ENST00000571721.5:c.364-10C>G	ENSP00000460660.1:n.364-10C>G
ENST00000572105.6:c.405-10C>G	ENSP00000462823.1:n.405-10C>G
ENST00000573283.5:c.364-10C>G	ENSP00000458435.1:n.364-10C>G
ENST00000574671.5:n.213C>G
ENST00000575087.5:c.364-10C>G	ENSP00000459124.1:n.364-10C>G
ENST00000575659.5:c.364-10C>G	ENSP00000459119.1:n.364-10C>G
ENST00000575842.5:c.364-10C>G	ENSP00000458162.1:n.364-10C>G
ENST00000575994.5:c.364-10C>G	ENSP00000460464.1:n.364-10C>G
ENST00000576209.5:n.249-10C>G
ENST00000576214.2:n.552C>G
ENST00000576544.5:c.364-10C>G	ENSP00000461672.1:n.364-10C>G
ENST00000576917.5:n.417-10C>G
ENST00000615544.4:c.364-10C>G	ENSP00000477968.1:n.364-10C>G
NM_001199954.1:c.364-10C>G	NP_001186883.1:n.364-10C>G
NM_001614.3:c.364-10C>G	NP_001605.1:n.364-10C>G
NR_037688.1:n.503-10C>G
NM_001199954.2:c.364-10C>G	NP_001186883.1:n.364-10C>G
NM_001614.4:c.364-10C>G	NP_001605.1:n.364-10C>G
NR_037688.2:n.436-10C>G
NM_001614.5:c.364-10C>G MANE Select	NP_001605.1:n.364-10C>G
NR_037688.3:n.436-10C>G
NM_001199954.3:c.364-10C>G	NP_001186883.1:n.364-10C>G