Canonical Allele Identifier: CA477369740

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968174C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097464C>T , CM000673.2:g.119097464C>T	GRCh38
NC_000011.9:g.118968174C>T , CM000673.1:g.118968174C>T	GRCh37
NC_000011.8:g.118473384C>T	NCBI36
NG_008918.1:g.9612G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1063G>A
ENST00000524658.2:n.1044G>A
ENST00000530052.2:n.2050G>A
ENST00000682191.1:n.1510G>A
ENST00000682192.1:n.1207G>A
ENST00000682232.1:c.*623-167G>A	ENSP00000507302.1:n.*623-167G>A
ENST00000682326.1:c.918-167G>A	ENSP00000508129.1:n.918-167G>A
ENST00000682404.1:n.2106G>A
ENST00000682517.1:n.2409G>A
ENST00000682652.1:n.2279G>A
ENST00000682665.1:n.1705G>A
ENST00000682691.1:n.1705G>A
ENST00000682791.1:c.918G>A	ENSP00000507312.1:p.Lys306=
ENST00000682811.1:c.*56G>A	ENSP00000508196.1:n.*56G>A
ENST00000682883.1:n.1032-167G>A
ENST00000682946.1:c.*87G>A	ENSP00000506856.1:n.*87G>A
ENST00000683143.1:c.*710G>A	ENSP00000507168.1:n.*710G>A
ENST00000683373.1:n.1510G>A
ENST00000683558.1:n.1510G>A
ENST00000683567.1:n.1114G>A
ENST00000683955.1:n.1761G>A
ENST00000684142.1:c.*680G>A	ENSP00000508008.1:n.*680G>A
ENST00000684252.1:n.1402G>A
ENST00000684255.1:c.*710G>A	ENSP00000507398.1:n.*710G>A
ENST00000684315.1:n.1738G>A
ENST00000684345.1:c.*983G>A	ENSP00000507163.1:n.*983G>A
ENST00000684499.1:c.*1110G>A	ENSP00000506800.1:n.*1110G>A
ENST00000684682.1:c.*736G>A	ENSP00000507326.1:n.*736G>A
ENST00000354202.9:c.1005G>A MANE Select	ENSP00000346142.4:p.Lys335=
ENST00000636404.1:c.233-401G>A
ENST00000638850.1:c.509G>A
ENST00000639704.1:c.912G>A	ENSP00000491336.1:p.Lys304=
ENST00000640102.1:c.*658G>A	ENSP00000492027.1:n.*658G>A
ENST00000640747.1:c.*680G>A	ENSP00000492730.1:n.*680G>A
ENST00000354202.8:c.1005G>A	ENSP00000346142.4:p.Lys335=
ENST00000392834.7:c.*710G>A	ENSP00000376579.3:n.*710G>A
ENST00000409993.6:c.1005G>A	ENSP00000386597.2:p.Lys335=
ENST00000414373.5:c.*475-167G>A	ENSP00000402019.1:n.*475-167G>A
ENST00000442480.1:c.737G>A	ENSP00000406591.1:n.737G>A
ENST00000461999.1:n.1172G>A
ENST00000481084.5:n.1634G>A
ENST00000524658.1:n.310G>A
ENST00000525456.5:n.819G>A
NM_001382.3:c.1005G>A	NP_001373.2:p.Lys335=
XM_005271422.2:c.1005G>A	XP_005271479.1:p.Lys335=
XM_011542648.1:c.684G>A	XP_011540950.1:p.Lys228=
XR_947801.1:n.1165-167G>A
XM_005271422.3:c.1005G>A	XP_005271479.1:p.Lys335=
XM_011542648.2:c.684G>A	XP_011540950.1:p.Lys228=
XM_017017293.2:c.684G>A	XP_016872782.1:p.Lys228=
XM_017017294.2:c.*87G>A	XP_016872783.1:n.*87G>A
XM_017017295.1:c.489G>A	XP_016872784.1:p.Lys163=
XR_001747785.2:n.1039G>A
XR_947801.2:n.952-167G>A
NM_001382.4:c.1005G>A MANE Select	NP_001373.2:p.Lys335=