Canonical Allele Identifier: CA401459531

Gene: ACTG1

Linked Data

• ClinVar Variation Id: 1312901
• ClinVar RCV Id: RCV001774355
• dbSNP Id: rs2143775987
• MyVariant Identifiers: chr17:g.79478132T>C (hg19) ; chr17:g.81511106T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511106T>C , CM000679.2:g.81511106T>C	GRCh38
NC_000017.10:g.79478132T>C , CM000679.1:g.79478132T>C	GRCh37
NC_000017.9:g.77092727T>C	NCBI36
NG_011433.1:g.6696A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000570382.2:c.805A>G	ENSP00000466346.2:p.Met269Val
ENST00000571691.6:c.733A>G	ENSP00000461407.2:p.Met245Val
ENST00000571721.6:c.805A>G	ENSP00000460660.2:p.Met269Val
ENST00000572105.7:c.*249A>G	ENSP00000462823.1:n.*249A>G
ENST00000573283.7:c.805A>G MANE Select	ENSP00000458435.1:p.Met269Val
ENST00000574671.6:n.1205A>G
ENST00000575659.6:c.805A>G	ENSP00000459119.2:p.Met269Val
ENST00000575994.6:c.805A>G	ENSP00000460464.2:p.Met269Val
ENST00000576214.3:n.1106A>G
ENST00000576544.6:c.805A>G	ENSP00000461672.1:p.Met269Val
ENST00000615544.5:c.805A>G	ENSP00000477968.1:p.Met269Val
ENST00000644774.2:c.778A>G	ENSP00000493648.2:p.Met260Val
ENST00000679410.1:n.1008A>G
ENST00000679480.1:c.805A>G	ENSP00000506201.1:p.Met269Val
ENST00000679535.1:n.1106A>G
ENST00000679778.1:c.805A>G	ENSP00000505235.1:p.Met269Val
ENST00000680227.1:c.805A>G	ENSP00000506253.1:p.Met269Val
ENST00000680727.1:c.805A>G	ENSP00000505193.1:p.Met269Val
ENST00000681052.1:c.805A>G	ENSP00000505060.1:p.Met269Val
ENST00000681092.1:c.*609A>G	ENSP00000506720.1:n.*609A>G
ENST00000681842.1:c.805A>G	ENSP00000506126.1:p.Met269Val
ENST00000331925.6:c.805A>G	ENSP00000331514.2:p.Met269Val
ENST00000572105.6:c.*249A>G	ENSP00000462823.1:n.*249A>G
ENST00000573283.5:c.805A>G	ENSP00000458435.1:p.Met269Val
ENST00000574671.5:n.664A>G
ENST00000575087.5:c.805A>G	ENSP00000459124.1:p.Met269Val
ENST00000575842.5:c.805A>G	ENSP00000458162.1:p.Met269Val
ENST00000576209.5:n.690A>G
ENST00000576214.2:n.1003A>G
ENST00000576544.5:c.805A>G	ENSP00000461672.1:p.Met269Val
ENST00000576917.5:n.937A>G
ENST00000615544.4:c.805A>G	ENSP00000477968.1:p.Met269Val
NM_001199954.1:c.805A>G	NP_001186883.1:p.Met269Val
NM_001614.3:c.805A>G	NP_001605.1:p.Met269Val
NR_037688.1:n.944A>G
NM_001199954.2:c.805A>G	NP_001186883.1:p.Met269Val
NM_001614.4:c.805A>G	NP_001605.1:p.Met269Val
NR_037688.2:n.877A>G
NM_001614.5:c.805A>G MANE Select	NP_001605.1:p.Met269Val
NR_037688.3:n.877A>G
NM_001199954.3:c.805A>G	NP_001186883.1:p.Met269Val