Canonical Allele Identifier: CA401460237

Gene: ACTG1

Linked Data

• ClinVar Variation Id: 1333818
• ClinVar RCV Id: RCV001809033 ; RCV004552031
• dbSNP Id: rs2143777781
• gnomAD v4: 17-81511335-C-T
• MyVariant Identifiers: chr17:g.79478361C>T (hg19) ; chr17:g.81511335C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511335C>T , CM000679.2:g.81511335C>T	GRCh38
NC_000017.10:g.79478361C>T , CM000679.1:g.79478361C>T	GRCh37
NC_000017.9:g.77092956C>T	NCBI36
NG_011433.1:g.6467G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.655G>A	ENSP00000466346.2:p.Val219Ile
ENST00000571691.6:c.583G>A	ENSP00000461407.2:p.Val195Ile
ENST00000571721.6:c.655G>A	ENSP00000460660.2:p.Val219Ile
ENST00000572105.7:c.*99G>A	ENSP00000462823.1:n.*99G>A
ENST00000573283.7:c.655G>A MANE Select	ENSP00000458435.1:p.Val219Ile
ENST00000574671.6:n.1055G>A
ENST00000575659.6:c.655G>A	ENSP00000459119.2:p.Val219Ile
ENST00000575994.6:c.655G>A	ENSP00000460464.2:p.Val219Ile
ENST00000576214.3:n.956G>A
ENST00000576544.6:c.655G>A	ENSP00000461672.1:p.Val219Ile
ENST00000615544.5:c.655G>A	ENSP00000477968.1:p.Val219Ile
ENST00000644774.2:c.628G>A	ENSP00000493648.2:p.Val210Ile
ENST00000679410.1:n.779G>A
ENST00000679480.1:c.655G>A	ENSP00000506201.1:p.Val219Ile
ENST00000679535.1:n.956G>A
ENST00000679778.1:c.655G>A	ENSP00000505235.1:p.Val219Ile
ENST00000680227.1:c.655G>A	ENSP00000506253.1:p.Val219Ile
ENST00000680727.1:c.655G>A	ENSP00000505193.1:p.Val219Ile
ENST00000681052.1:c.655G>A	ENSP00000505060.1:p.Val219Ile
ENST00000681092.1:c.*459G>A	ENSP00000506720.1:n.*459G>A
ENST00000681842.1:c.655G>A	ENSP00000506126.1:p.Val219Ile
ENST00000331925.6:c.655G>A	ENSP00000331514.2:p.Val219Ile
ENST00000571691.5:c.628G>A	ENSP00000461407.1:p.Val210Ile
ENST00000572105.6:c.*99G>A	ENSP00000462823.1:n.*99G>A
ENST00000573283.5:c.655G>A	ENSP00000458435.1:p.Val219Ile
ENST00000574671.5:n.514G>A
ENST00000575087.5:c.655G>A	ENSP00000459124.1:p.Val219Ile
ENST00000575842.5:c.655G>A	ENSP00000458162.1:p.Val219Ile
ENST00000576209.5:n.540G>A
ENST00000576214.2:n.853G>A
ENST00000576544.5:c.655G>A	ENSP00000461672.1:p.Val219Ile
ENST00000576917.5:n.708G>A
ENST00000615544.4:c.655G>A	ENSP00000477968.1:p.Val219Ile
NM_001199954.1:c.655G>A	NP_001186883.1:p.Val219Ile
NM_001614.3:c.655G>A	NP_001605.1:p.Val219Ile
NR_037688.1:n.794G>A
NM_001199954.2:c.655G>A	NP_001186883.1:p.Val219Ile
NM_001614.4:c.655G>A	NP_001605.1:p.Val219Ile
NR_037688.2:n.727G>A
NM_001614.5:c.655G>A MANE Select	NP_001605.1:p.Val219Ile
NR_037688.3:n.727G>A
NM_001199954.3:c.655G>A	NP_001186883.1:p.Val219Ile