Canonical Allele Identifier: CA382909433

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968181A>T (hg19) ; chr11:g.119097471A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097471A>T , CM000673.2:g.119097471A>T	GRCh38
NC_000011.9:g.118968181A>T , CM000673.1:g.118968181A>T	GRCh37
NC_000011.8:g.118473391A>T	NCBI36
NG_008918.1:g.9605T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1056T>A
ENST00000524658.2:n.1037T>A
ENST00000530052.2:n.2043T>A
ENST00000682191.1:n.1503T>A
ENST00000682192.1:n.1200T>A
ENST00000682232.1:c.*623-174T>A	ENSP00000507302.1:n.*623-174T>A
ENST00000682326.1:c.918-174T>A	ENSP00000508129.1:n.918-174T>A
ENST00000682404.1:n.2099T>A
ENST00000682517.1:n.2402T>A
ENST00000682652.1:n.2272T>A
ENST00000682665.1:n.1698T>A
ENST00000682691.1:n.1698T>A
ENST00000682791.1:c.911T>A	ENSP00000507312.1:p.Ile304Asn
ENST00000682811.1:c.*49T>A	ENSP00000508196.1:n.*49T>A
ENST00000682883.1:n.1032-174T>A
ENST00000682946.1:c.*80T>A	ENSP00000506856.1:n.*80T>A
ENST00000683143.1:c.*703T>A	ENSP00000507168.1:n.*703T>A
ENST00000683373.1:n.1503T>A
ENST00000683558.1:n.1503T>A
ENST00000683567.1:n.1107T>A
ENST00000683955.1:n.1754T>A
ENST00000684142.1:c.*673T>A	ENSP00000508008.1:n.*673T>A
ENST00000684252.1:n.1395T>A
ENST00000684255.1:c.*703T>A	ENSP00000507398.1:n.*703T>A
ENST00000684315.1:n.1731T>A
ENST00000684345.1:c.*976T>A	ENSP00000507163.1:n.*976T>A
ENST00000684499.1:c.*1103T>A	ENSP00000506800.1:n.*1103T>A
ENST00000684682.1:c.*729T>A	ENSP00000507326.1:n.*729T>A
ENST00000354202.9:c.998T>A MANE Select	ENSP00000346142.4:p.Ile333Asn
ENST00000636404.1:c.233-408T>A
ENST00000638850.1:c.502T>A
ENST00000639704.1:c.905T>A	ENSP00000491336.1:p.Ile302Asn
ENST00000640102.1:c.*651T>A	ENSP00000492027.1:n.*651T>A
ENST00000640747.1:c.*673T>A	ENSP00000492730.1:n.*673T>A
ENST00000354202.8:c.998T>A	ENSP00000346142.4:p.Ile333Asn
ENST00000392834.7:c.*703T>A	ENSP00000376579.3:n.*703T>A
ENST00000409993.6:c.998T>A	ENSP00000386597.2:p.Ile333Asn
ENST00000414373.5:c.*475-174T>A	ENSP00000402019.1:n.*475-174T>A
ENST00000442480.1:c.730T>A	ENSP00000406591.1:n.730T>A
ENST00000461999.1:n.1165T>A
ENST00000481084.5:n.1627T>A
ENST00000524658.1:n.303T>A
ENST00000525456.5:n.812T>A
NM_001382.3:c.998T>A	NP_001373.2:p.Ile333Asn
XM_005271422.2:c.998T>A	XP_005271479.1:p.Ile333Asn
XM_011542648.1:c.677T>A	XP_011540950.1:p.Ile226Asn
XR_947801.1:n.1165-174T>A
XM_005271422.3:c.998T>A	XP_005271479.1:p.Ile333Asn
XM_011542648.2:c.677T>A	XP_011540950.1:p.Ile226Asn
XM_017017293.2:c.677T>A	XP_016872782.1:p.Ile226Asn
XM_017017294.2:c.*80T>A	XP_016872783.1:n.*80T>A
XM_017017295.1:c.482T>A	XP_016872784.1:p.Ile161Asn
XR_001747785.2:n.1032T>A
XR_947801.2:n.952-174T>A
NM_001382.4:c.998T>A MANE Select	NP_001373.2:p.Ile333Asn