Canonical Allele Identifier: CA401458755

Gene: ACTG1

Linked Data

• MyVariant Identifiers: chr17:g.79477957A>C (hg19) ; chr17:g.81510931A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81510931A>C , CM000679.2:g.81510931A>C	GRCh38
NC_000017.10:g.79477957A>C , CM000679.1:g.79477957A>C	GRCh37
NC_000017.9:g.77092552A>C	NCBI36
NG_011433.1:g.6871T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570382.2:c.980T>G	ENSP00000466346.2:p.Ile327Ser
ENST00000571691.6:c.908T>G	ENSP00000461407.2:p.Ile303Ser
ENST00000571721.6:c.980T>G	ENSP00000460660.2:p.Ile327Ser
ENST00000572105.7:c.*424T>G	ENSP00000462823.1:n.*424T>G
ENST00000573283.7:c.980T>G MANE Select	ENSP00000458435.1:p.Ile327Ser
ENST00000574671.6:n.1380T>G
ENST00000575659.6:c.980T>G	ENSP00000459119.2:p.Ile327Ser
ENST00000575994.6:c.980T>G	ENSP00000460464.2:p.Ile327Ser
ENST00000576214.3:n.1281T>G
ENST00000576544.6:c.980T>G	ENSP00000461672.1:p.Ile327Ser
ENST00000615544.5:c.980T>G	ENSP00000477968.1:p.Ile327Ser
ENST00000644774.2:c.953T>G	ENSP00000493648.2:p.Ile318Ser
ENST00000679410.1:n.1183T>G
ENST00000679480.1:c.980T>G	ENSP00000506201.1:p.Ile327Ser
ENST00000679535.1:n.1281T>G
ENST00000679778.1:c.980T>G	ENSP00000505235.1:p.Ile327Ser
ENST00000680227.1:c.980T>G	ENSP00000506253.1:p.Ile327Ser
ENST00000680727.1:c.980T>G	ENSP00000505193.1:p.Ile327Ser
ENST00000681052.1:c.980T>G	ENSP00000505060.1:p.Ile327Ser
ENST00000681092.1:c.*784T>G	ENSP00000506720.1:n.*784T>G
ENST00000681842.1:c.980T>G	ENSP00000506126.1:p.Ile327Ser
ENST00000331925.6:c.980T>G	ENSP00000331514.2:p.Ile327Ser
ENST00000572105.6:c.*424T>G	ENSP00000462823.1:n.*424T>G
ENST00000573283.5:c.980T>G	ENSP00000458435.1:p.Ile327Ser
ENST00000574671.5:n.839T>G
ENST00000575087.5:c.980T>G	ENSP00000459124.1:p.Ile327Ser
ENST00000575842.5:c.980T>G	ENSP00000458162.1:p.Ile327Ser
ENST00000576209.5:n.865T>G
ENST00000576544.5:c.980T>G	ENSP00000461672.1:p.Ile327Ser
ENST00000576917.5:n.1112T>G
ENST00000615544.4:c.980T>G	ENSP00000477968.1:p.Ile327Ser
NM_001199954.1:c.980T>G	NP_001186883.1:p.Ile327Ser
NM_001614.3:c.980T>G	NP_001605.1:p.Ile327Ser
NR_037688.1:n.1119T>G
NM_001199954.2:c.980T>G	NP_001186883.1:p.Ile327Ser
NM_001614.4:c.980T>G	NP_001605.1:p.Ile327Ser
NR_037688.2:n.1052T>G
NM_001614.5:c.980T>G MANE Select	NP_001605.1:p.Ile327Ser
NR_037688.3:n.1052T>G
NM_001199954.3:c.980T>G	NP_001186883.1:p.Ile327Ser