Canonical Allele Identifier: CA401459632
Gene: ACTG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.79478214C>T (hg19) chr17:g.81511188C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81511188C>T , CM000679.2:g.81511188C>T GRCh38
NC_000017.10:g.79478214C>T , CM000679.1:g.79478214C>T GRCh37
NC_000017.9:g.77092809C>T NCBI36
NG_011433.1:g.6614G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000570382.2:c.802G>A ENSP00000466346.2:p.Gly268Ser
ENST00000571691.6:c.730G>A ENSP00000461407.2:p.Gly244Ser
ENST00000571721.6:c.802G>A ENSP00000460660.2:p.Gly268Ser
ENST00000572105.7:c.*246G>A ENSP00000462823.1:n.*246G>A
ENST00000573283.7:c.802G>A MANE Select ENSP00000458435.1:p.Gly268Ser
ENST00000574671.6:n.1202G>A
ENST00000575659.6:c.802G>A ENSP00000459119.2:p.Gly268Ser
ENST00000575994.6:c.802G>A ENSP00000460464.2:p.Gly268Ser
ENST00000576214.3:n.1103G>A
ENST00000576544.6:c.802G>A ENSP00000461672.1:p.Gly268Ser
ENST00000615544.5:c.802G>A ENSP00000477968.1:p.Gly268Ser
ENST00000644774.2:c.775G>A ENSP00000493648.2:p.Gly259Ser
ENST00000679410.1:n.926G>A
ENST00000679480.1:c.802G>A ENSP00000506201.1:p.Gly268Ser
ENST00000679535.1:n.1103G>A
ENST00000679778.1:c.802G>A ENSP00000505235.1:p.Gly268Ser
ENST00000680227.1:c.802G>A ENSP00000506253.1:p.Gly268Ser
ENST00000680727.1:c.802G>A ENSP00000505193.1:p.Gly268Ser
ENST00000681052.1:c.802G>A ENSP00000505060.1:p.Gly268Ser
ENST00000681092.1:c.*606G>A ENSP00000506720.1:n.*606G>A
ENST00000681842.1:c.802G>A ENSP00000506126.1:p.Gly268Ser
ENST00000331925.6:c.802G>A ENSP00000331514.2:p.Gly268Ser
ENST00000572105.6:c.*246G>A ENSP00000462823.1:n.*246G>A
ENST00000573283.5:c.802G>A ENSP00000458435.1:p.Gly268Ser
ENST00000574671.5:n.661G>A
ENST00000575087.5:c.802G>A ENSP00000459124.1:p.Gly268Ser
ENST00000575842.5:c.802G>A ENSP00000458162.1:p.Gly268Ser
ENST00000576209.5:n.687G>A
ENST00000576214.2:n.1000G>A
ENST00000576544.5:c.802G>A ENSP00000461672.1:p.Gly268Ser
ENST00000576917.5:n.855G>A
ENST00000615544.4:c.802G>A ENSP00000477968.1:p.Gly268Ser
NM_001199954.1:c.802G>A NP_001186883.1:p.Gly268Ser
NM_001614.3:c.802G>A NP_001605.1:p.Gly268Ser
NR_037688.1:n.941G>A
NM_001199954.2:c.802G>A NP_001186883.1:p.Gly268Ser
NM_001614.4:c.802G>A NP_001605.1:p.Gly268Ser
NR_037688.2:n.874G>A
NM_001614.5:c.802G>A MANE Select NP_001605.1:p.Gly268Ser
NR_037688.3:n.874G>A
NM_001199954.3:c.802G>A NP_001186883.1:p.Gly268Ser
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