Canonical Allele Identifier: CA502419367

Gene: ACTG1

Linked Data

• ClinVar Variation Id: 1879387
• ClinVar RCV Id: RCV002511886
• dbSNP Id: rs1568061170
• gnomAD v4: 17-81511288-A-G
• MyVariant Identifiers: chr17:g.79478314A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511288A>G , CM000679.2:g.81511288A>G	GRCh38
NC_000017.10:g.79478314A>G , CM000679.1:g.79478314A>G	GRCh37
NC_000017.9:g.77092909A>G	NCBI36
NG_011433.1:g.6514T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000570382.2:c.702T>C	ENSP00000466346.2:p.Ser234=
ENST00000571691.6:c.630T>C	ENSP00000461407.2:p.Ser210=
ENST00000571721.6:c.702T>C	ENSP00000460660.2:p.Ser234=
ENST00000572105.7:c.*146T>C	ENSP00000462823.1:n.*146T>C
ENST00000573283.7:c.702T>C MANE Select	ENSP00000458435.1:p.Ser234=
ENST00000574671.6:n.1102T>C
ENST00000575659.6:c.702T>C	ENSP00000459119.2:p.Ser234=
ENST00000575994.6:c.702T>C	ENSP00000460464.2:p.Ser234=
ENST00000576214.3:n.1003T>C
ENST00000576544.6:c.702T>C	ENSP00000461672.1:p.Ser234=
ENST00000615544.5:c.702T>C	ENSP00000477968.1:p.Ser234=
ENST00000644774.2:c.675T>C	ENSP00000493648.2:p.Ser225=
ENST00000679410.1:n.826T>C
ENST00000679480.1:c.702T>C	ENSP00000506201.1:p.Ser234=
ENST00000679535.1:n.1003T>C
ENST00000679778.1:c.702T>C	ENSP00000505235.1:p.Ser234=
ENST00000680227.1:c.702T>C	ENSP00000506253.1:p.Ser234=
ENST00000680727.1:c.702T>C	ENSP00000505193.1:p.Ser234=
ENST00000681052.1:c.702T>C	ENSP00000505060.1:p.Ser234=
ENST00000681092.1:c.*506T>C	ENSP00000506720.1:n.*506T>C
ENST00000681842.1:c.702T>C	ENSP00000506126.1:p.Ser234=
ENST00000331925.6:c.702T>C	ENSP00000331514.2:p.Ser234=
ENST00000571691.5:c.675T>C	ENSP00000461407.1:p.Ser225=
ENST00000572105.6:c.*146T>C	ENSP00000462823.1:n.*146T>C
ENST00000573283.5:c.702T>C	ENSP00000458435.1:p.Ser234=
ENST00000574671.5:n.561T>C
ENST00000575087.5:c.702T>C	ENSP00000459124.1:p.Ser234=
ENST00000575842.5:c.702T>C	ENSP00000458162.1:p.Ser234=
ENST00000576209.5:n.587T>C
ENST00000576214.2:n.900T>C
ENST00000576544.5:c.702T>C	ENSP00000461672.1:p.Ser234=
ENST00000576917.5:n.755T>C
ENST00000615544.4:c.702T>C	ENSP00000477968.1:p.Ser234=
NM_001199954.1:c.702T>C	NP_001186883.1:p.Ser234=
NM_001614.3:c.702T>C	NP_001605.1:p.Ser234=
NR_037688.1:n.841T>C
NM_001199954.2:c.702T>C	NP_001186883.1:p.Ser234=
NM_001614.4:c.702T>C	NP_001605.1:p.Ser234=
NR_037688.2:n.774T>C
NM_001614.5:c.702T>C MANE Select	NP_001605.1:p.Ser234=
NR_037688.3:n.774T>C
NM_001199954.3:c.702T>C	NP_001186883.1:p.Ser234=