Canonical Allele Identifier: CA775646512

Gene: ACTG1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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