Canonical Allele Identifier: CA382909958

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968230T>A (hg19) ; chr11:g.119097520T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097520T>A , CM000673.2:g.119097520T>A	GRCh38
NC_000011.9:g.118968230T>A , CM000673.1:g.118968230T>A	GRCh37
NC_000011.8:g.118473440T>A	NCBI36
NG_008918.1:g.9556A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1007A>T
ENST00000524658.2:n.988A>T
ENST00000530052.2:n.1994A>T
ENST00000682191.1:n.1454A>T
ENST00000682192.1:n.1151A>T
ENST00000682232.1:c.*623-223A>T	ENSP00000507302.1:n.*623-223A>T
ENST00000682326.1:c.918-223A>T	ENSP00000508129.1:n.918-223A>T
ENST00000682404.1:n.2050A>T
ENST00000682517.1:n.2353A>T
ENST00000682652.1:n.2223A>T
ENST00000682665.1:n.1649A>T
ENST00000682691.1:n.1649A>T
ENST00000682791.1:c.862A>T	ENSP00000507312.1:p.Ser288Cys
ENST00000682811.1:c.831A>T	ENSP00000508196.1:p.Ter277Cys
ENST00000682883.1:n.1032-223A>T
ENST00000682946.1:c.*31A>T	ENSP00000506856.1:n.*31A>T
ENST00000683143.1:c.*654A>T	ENSP00000507168.1:n.*654A>T
ENST00000683373.1:n.1454A>T
ENST00000683558.1:n.1454A>T
ENST00000683567.1:n.1058A>T
ENST00000683955.1:n.1705A>T
ENST00000684142.1:c.*624A>T	ENSP00000508008.1:n.*624A>T
ENST00000684252.1:n.1346A>T
ENST00000684255.1:c.*654A>T	ENSP00000507398.1:n.*654A>T
ENST00000684315.1:n.1682A>T
ENST00000684345.1:c.*927A>T	ENSP00000507163.1:n.*927A>T
ENST00000684499.1:c.*1054A>T	ENSP00000506800.1:n.*1054A>T
ENST00000684682.1:c.*680A>T	ENSP00000507326.1:n.*680A>T
ENST00000354202.9:c.949A>T MANE Select	ENSP00000346142.4:p.Ser317Cys
ENST00000636404.1:c.233-457A>T
ENST00000638850.1:c.453A>T
ENST00000639704.1:c.856A>T	ENSP00000491336.1:p.Ser286Cys
ENST00000640102.1:c.*602A>T	ENSP00000492027.1:n.*602A>T
ENST00000640747.1:c.*624A>T	ENSP00000492730.1:n.*624A>T
ENST00000354202.8:c.949A>T	ENSP00000346142.4:p.Ser317Cys
ENST00000392834.7:c.*654A>T	ENSP00000376579.3:n.*654A>T
ENST00000409993.6:c.949A>T	ENSP00000386597.2:p.Ser317Cys
ENST00000414373.5:c.*475-223A>T	ENSP00000402019.1:n.*475-223A>T
ENST00000442480.1:c.681A>T	ENSP00000406591.1:p.Ter227Cys
ENST00000461999.1:n.1116A>T
ENST00000481084.5:n.1578A>T
ENST00000524658.1:n.254A>T
ENST00000525456.5:n.763A>T
NM_001382.3:c.949A>T	NP_001373.2:p.Ser317Cys
XM_005271422.2:c.949A>T	XP_005271479.1:p.Ser317Cys
XM_011542648.1:c.628A>T	XP_011540950.1:p.Ser210Cys
XR_947801.1:n.1165-223A>T
XM_005271422.3:c.949A>T	XP_005271479.1:p.Ser317Cys
XM_011542648.2:c.628A>T	XP_011540950.1:p.Ser210Cys
XM_017017293.2:c.628A>T	XP_016872782.1:p.Ser210Cys
XM_017017294.2:c.*31A>T	XP_016872783.1:n.*31A>T
XM_017017295.1:c.433A>T	XP_016872784.1:p.Ser145Cys
XR_001747785.2:n.983A>T
XR_947801.2:n.952-223A>T
NM_001382.4:c.949A>T MANE Select	NP_001373.2:p.Ser317Cys