Canonical Allele Identifier: CA477369750

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968189G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097479G>T , CM000673.2:g.119097479G>T	GRCh38
NC_000011.9:g.118968189G>T , CM000673.1:g.118968189G>T	GRCh37
NC_000011.8:g.118473399G>T	NCBI36
NG_008918.1:g.9597C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1048C>A
ENST00000524658.2:n.1029C>A
ENST00000530052.2:n.2035C>A
ENST00000682191.1:n.1495C>A
ENST00000682192.1:n.1192C>A
ENST00000682232.1:c.*623-182C>A	ENSP00000507302.1:n.*623-182C>A
ENST00000682326.1:c.918-182C>A	ENSP00000508129.1:n.918-182C>A
ENST00000682404.1:n.2091C>A
ENST00000682517.1:n.2394C>A
ENST00000682652.1:n.2264C>A
ENST00000682665.1:n.1690C>A
ENST00000682691.1:n.1690C>A
ENST00000682791.1:c.903C>A	ENSP00000507312.1:p.Gly301=
ENST00000682811.1:c.*41C>A	ENSP00000508196.1:n.*41C>A
ENST00000682883.1:n.1032-182C>A
ENST00000682946.1:c.*72C>A	ENSP00000506856.1:n.*72C>A
ENST00000683143.1:c.*695C>A	ENSP00000507168.1:n.*695C>A
ENST00000683373.1:n.1495C>A
ENST00000683558.1:n.1495C>A
ENST00000683567.1:n.1099C>A
ENST00000683955.1:n.1746C>A
ENST00000684142.1:c.*665C>A	ENSP00000508008.1:n.*665C>A
ENST00000684252.1:n.1387C>A
ENST00000684255.1:c.*695C>A	ENSP00000507398.1:n.*695C>A
ENST00000684315.1:n.1723C>A
ENST00000684345.1:c.*968C>A	ENSP00000507163.1:n.*968C>A
ENST00000684499.1:c.*1095C>A	ENSP00000506800.1:n.*1095C>A
ENST00000684682.1:c.*721C>A	ENSP00000507326.1:n.*721C>A
ENST00000354202.9:c.990C>A MANE Select	ENSP00000346142.4:p.Gly330=
ENST00000636404.1:c.233-416C>A
ENST00000638850.1:c.494C>A
ENST00000639704.1:c.897C>A	ENSP00000491336.1:p.Gly299=
ENST00000640102.1:c.*643C>A	ENSP00000492027.1:n.*643C>A
ENST00000640747.1:c.*665C>A	ENSP00000492730.1:n.*665C>A
ENST00000354202.8:c.990C>A	ENSP00000346142.4:p.Gly330=
ENST00000392834.7:c.*695C>A	ENSP00000376579.3:n.*695C>A
ENST00000409993.6:c.990C>A	ENSP00000386597.2:p.Gly330=
ENST00000414373.5:c.*475-182C>A	ENSP00000402019.1:n.*475-182C>A
ENST00000442480.1:c.722C>A	ENSP00000406591.1:n.722C>A
ENST00000461999.1:n.1157C>A
ENST00000481084.5:n.1619C>A
ENST00000524658.1:n.295C>A
ENST00000525456.5:n.804C>A
NM_001382.3:c.990C>A	NP_001373.2:p.Gly330=
XM_005271422.2:c.990C>A	XP_005271479.1:p.Gly330=
XM_011542648.1:c.669C>A	XP_011540950.1:p.Gly223=
XR_947801.1:n.1165-182C>A
XM_005271422.3:c.990C>A	XP_005271479.1:p.Gly330=
XM_011542648.2:c.669C>A	XP_011540950.1:p.Gly223=
XM_017017293.2:c.669C>A	XP_016872782.1:p.Gly223=
XM_017017294.2:c.*72C>A	XP_016872783.1:n.*72C>A
XM_017017295.1:c.474C>A	XP_016872784.1:p.Gly158=
XR_001747785.2:n.1024C>A
XR_947801.2:n.952-182C>A
NM_001382.4:c.990C>A MANE Select	NP_001373.2:p.Gly330=