Canonical Allele Identifier: CA775646513

Gene: ACTG1

Linked Data

• dbSNP Id: rs1156369373
• gnomAD v3: 17-81512802-C-G
• gnomAD v4: 17-81512802-C-G
• MyVariant Identifiers: chr17:g.81512802C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81512802C>G , CM000679.2:g.81512802C>G	GRCh38
NC_000017.10:g.79479828C>G , CM000679.1:g.79479828C>G	GRCh37
NC_000017.9:g.77094423C>G	NCBI36
NG_011433.1:g.5000G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.-194G>C	ENSP00000466346.2:n.-194G>C
ENST00000572105.7:c.-75G>C	ENSP00000462823.1:n.-75G>C
ENST00000574671.6:n.50G>C
ENST00000575659.6:c.-6-442G>C	ENSP00000459119.2:n.-6-442G>C
ENST00000575994.6:c.-6-442G>C	ENSP00000460464.2:n.-6-442G>C
ENST00000576214.3:n.50G>C
ENST00000576544.6:c.-75G>C	ENSP00000461672.1:n.-75G>C
ENST00000615544.5:c.-6-442G>C	ENSP00000477968.1:n.-6-442G>C
ENST00000679410.1:n.50G>C
ENST00000679535.1:n.50G>C
ENST00000679778.1:c.-6-442G>C	ENSP00000505235.1:n.-6-442G>C
ENST00000681052.1:c.-67-8G>C	ENSP00000505060.1:n.-67-8G>C
ENST00000681842.1:c.-75G>C	ENSP00000506126.1:n.-75G>C
ENST00000331925.6:c.-75G>C	ENSP00000331514.2:n.-75G>C
ENST00000575659.5:c.-6-442G>C	ENSP00000459119.1:n.-6-442G>C
ENST00000575994.5:c.-6-442G>C	ENSP00000460464.1:n.-6-442G>C
NM_001199954.1:c.-194G>C	NP_001186883.1:n.-194G>C
NM_001614.3:c.-75G>C	NP_001605.1:n.-75G>C
NR_037688.1:n.65G>C