Canonical Allele Identifier: CA775646509

Gene: ACTG1

Linked Data

• dbSNP Id: rs1289794642
• gnomAD v4: 17-81512800-A-C
• MyVariant Identifiers: chr17:g.81512800A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81512800A>C , CM000679.2:g.81512800A>C	GRCh38
NC_000017.10:g.79479826A>C , CM000679.1:g.79479826A>C	GRCh37
NC_000017.9:g.77094421A>C	NCBI36
NG_011433.1:g.5002T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.-192T>G	ENSP00000466346.2:n.-192T>G
ENST00000572105.7:c.-73T>G	ENSP00000462823.1:n.-73T>G
ENST00000574671.6:n.52T>G
ENST00000575659.6:c.-6-440T>G	ENSP00000459119.2:n.-6-440T>G
ENST00000575994.6:c.-6-440T>G	ENSP00000460464.2:n.-6-440T>G
ENST00000576214.3:n.52T>G
ENST00000576544.6:c.-73T>G	ENSP00000461672.1:n.-73T>G
ENST00000615544.5:c.-6-440T>G	ENSP00000477968.1:n.-6-440T>G
ENST00000679410.1:n.52T>G
ENST00000679535.1:n.52T>G
ENST00000679778.1:c.-6-440T>G	ENSP00000505235.1:n.-6-440T>G
ENST00000681052.1:c.-67-6T>G	ENSP00000505060.1:n.-67-6T>G
ENST00000681092.1:c.-73T>G	ENSP00000506720.1:n.-73T>G
ENST00000681842.1:c.-73T>G	ENSP00000506126.1:n.-73T>G
ENST00000331925.6:c.-73T>G	ENSP00000331514.2:n.-73T>G
ENST00000575659.5:c.-6-440T>G	ENSP00000459119.1:n.-6-440T>G
ENST00000575994.5:c.-6-440T>G	ENSP00000460464.1:n.-6-440T>G
NM_001199954.1:c.-192T>G	NP_001186883.1:n.-192T>G
NM_001614.3:c.-73T>G	NP_001605.1:n.-73T>G
NR_037688.1:n.67T>G