Canonical Allele Identifier: CA295068313

Gene: ACTG1

Linked Data

• dbSNP Id: rs147475815
• gnomAD v3: 17-81511351-C-T
• gnomAD v4: 17-81511351-C-T
• MyVariant Identifiers: chr17:g.79478377C>T (hg19) ; chr17:g.81511351C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81511351C>T , CM000679.2:g.81511351C>T	GRCh38
NC_000017.10:g.79478377C>T , CM000679.1:g.79478377C>T	GRCh37
NC_000017.9:g.77092972C>T	NCBI36
NG_011433.1:g.6451G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.639G>A	ENSP00000466346.2:p.Lys213=
ENST00000571691.6:c.567G>A	ENSP00000461407.2:p.Lys189=
ENST00000571721.6:c.639G>A	ENSP00000460660.2:p.Lys213=
ENST00000572105.7:c.*83G>A	ENSP00000462823.1:n.*83G>A
ENST00000573283.7:c.639G>A MANE Select	ENSP00000458435.1:p.Lys213=
ENST00000574671.6:n.1039G>A
ENST00000575659.6:c.639G>A	ENSP00000459119.2:p.Lys213=
ENST00000575994.6:c.639G>A	ENSP00000460464.2:p.Lys213=
ENST00000576214.3:n.940G>A
ENST00000576544.6:c.639G>A	ENSP00000461672.1:p.Lys213=
ENST00000615544.5:c.639G>A	ENSP00000477968.1:p.Lys213=
ENST00000644774.2:c.612G>A	ENSP00000493648.2:p.Lys204=
ENST00000679410.1:n.763G>A
ENST00000679480.1:c.639G>A	ENSP00000506201.1:p.Lys213=
ENST00000679535.1:n.940G>A
ENST00000679778.1:c.639G>A	ENSP00000505235.1:p.Lys213=
ENST00000680227.1:c.639G>A	ENSP00000506253.1:p.Lys213=
ENST00000680727.1:c.639G>A	ENSP00000505193.1:p.Lys213=
ENST00000681052.1:c.639G>A	ENSP00000505060.1:p.Lys213=
ENST00000681092.1:c.*443G>A	ENSP00000506720.1:n.*443G>A
ENST00000681842.1:c.639G>A	ENSP00000506126.1:p.Lys213=
ENST00000331925.6:c.639G>A	ENSP00000331514.2:p.Lys213=
ENST00000571691.5:c.612G>A	ENSP00000461407.1:p.Lys204=
ENST00000572105.6:c.*83G>A	ENSP00000462823.1:n.*83G>A
ENST00000573283.5:c.639G>A	ENSP00000458435.1:p.Lys213=
ENST00000574671.5:n.498G>A
ENST00000575087.5:c.639G>A	ENSP00000459124.1:p.Lys213=
ENST00000575659.5:c.639G>A	ENSP00000459119.1:p.Lys213=
ENST00000575842.5:c.639G>A	ENSP00000458162.1:p.Lys213=
ENST00000575994.5:c.639G>A	ENSP00000460464.1:p.Lys213=
ENST00000576209.5:n.524G>A
ENST00000576214.2:n.837G>A
ENST00000576544.5:c.639G>A	ENSP00000461672.1:p.Lys213=
ENST00000576917.5:n.692G>A
ENST00000615544.4:c.639G>A	ENSP00000477968.1:p.Lys213=
NM_001199954.1:c.639G>A	NP_001186883.1:p.Lys213=
NM_001614.3:c.639G>A	NP_001605.1:p.Lys213=
NR_037688.1:n.778G>A
NM_001199954.2:c.639G>A	NP_001186883.1:p.Lys213=
NM_001614.4:c.639G>A	NP_001605.1:p.Lys213=
NR_037688.2:n.711G>A
NM_001614.5:c.639G>A MANE Select	NP_001605.1:p.Lys213=
NR_037688.3:n.711G>A
NM_001199954.3:c.639G>A	NP_001186883.1:p.Lys213=