Canonical Allele Identifier: CA627771888

Gene: ACTG1

Linked Data

• dbSNP Id: rs1555667574
• gnomAD v2: 17-79479804-A-G
• gnomAD v3: 17-81512778-A-G
• gnomAD v4: 17-81512778-A-G
• MyVariant Identifiers: chr17:g.79479804A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81512778A>G , CM000679.2:g.81512778A>G	GRCh38
NC_000017.10:g.79479804A>G , CM000679.1:g.79479804A>G	GRCh37
NC_000017.9:g.77094399A>G	NCBI36
NG_011433.1:g.5024T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.-170T>C	ENSP00000466346.2:n.-170T>C
ENST00000571691.6:c.-51T>C	ENSP00000461407.2:n.-51T>C
ENST00000571721.6:c.-321T>C	ENSP00000460660.2:n.-321T>C
ENST00000572105.7:c.-51T>C	ENSP00000462823.1:n.-51T>C
ENST00000573283.7:c.-51T>C MANE Select	ENSP00000458435.1:n.-51T>C
ENST00000574671.6:n.74T>C
ENST00000575659.6:c.-6-418T>C	ENSP00000459119.2:n.-6-418T>C
ENST00000575994.6:c.-6-418T>C	ENSP00000460464.2:n.-6-418T>C
ENST00000576214.3:n.74T>C
ENST00000576544.6:c.-51T>C	ENSP00000461672.1:n.-51T>C
ENST00000615544.5:c.-6-418T>C	ENSP00000477968.1:n.-6-418T>C
ENST00000679410.1:n.74T>C
ENST00000679535.1:n.74T>C
ENST00000679778.1:c.-6-418T>C	ENSP00000505235.1:n.-6-418T>C
ENST00000681052.1:c.-51T>C	ENSP00000505060.1:n.-51T>C
ENST00000681092.1:c.-51T>C	ENSP00000506720.1:n.-51T>C
ENST00000681842.1:c.-51T>C	ENSP00000506126.1:n.-51T>C
ENST00000331925.6:c.-51T>C	ENSP00000331514.2:n.-51T>C
ENST00000570382.1:c.-51T>C	ENSP00000466346.1:n.-51T>C
ENST00000571721.5:c.-321T>C	ENSP00000460660.1:n.-321T>C
ENST00000572105.6:c.-51T>C	ENSP00000462823.1:n.-51T>C
ENST00000573283.5:c.-170T>C	ENSP00000458435.1:n.-170T>C
ENST00000575087.5:c.-179T>C	ENSP00000459124.1:n.-179T>C
ENST00000575659.5:c.-6-418T>C	ENSP00000459119.1:n.-6-418T>C
ENST00000575842.5:c.-424T>C	ENSP00000458162.1:n.-424T>C
ENST00000575994.5:c.-6-418T>C	ENSP00000460464.1:n.-6-418T>C
ENST00000576544.5:c.-51T>C	ENSP00000461672.1:n.-51T>C
ENST00000576917.5:n.3T>C
NM_001199954.1:c.-170T>C	NP_001186883.1:n.-170T>C
NM_001614.3:c.-51T>C	NP_001605.1:n.-51T>C
NR_037688.1:n.89T>C
NM_001199954.2:c.-170T>C	NP_001186883.1:n.-170T>C
NM_001614.4:c.-51T>C	NP_001605.1:n.-51T>C
NR_037688.2:n.22T>C
NM_001614.5:c.-51T>C MANE Select	NP_001605.1:n.-51T>C
NR_037688.3:n.22T>C
NM_001199954.3:c.-170T>C	NP_001186883.1:n.-170T>C