Canonical Allele Identifier: CA2003808815
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097453T= , CM000673.2:g.119097453T= GRCh38
NC_000011.9:g.118968163T= , CM000673.1:g.118968163T= GRCh37
NC_000011.8:g.118473373T= NCBI36
NG_008918.1:g.9623A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.1074A=
ENST00000524658.2:n.1055A=
ENST00000530052.2:n.2061A=
ENST00000682191.1:n.1510+11A=
ENST00000682192.1:n.1218A=
ENST00000682232.1:c.*623-156A= ENSP00000507302.1:n.*623-156A=
ENST00000682326.1:c.918-156A= ENSP00000508129.1:n.918-156A=
ENST00000682404.1:n.2117A=
ENST00000682517.1:n.2420A=
ENST00000682652.1:n.2279+11A=
ENST00000682665.1:n.1716A=
ENST00000682691.1:n.1716A=
ENST00000682791.1:c.918+11A= ENSP00000507312.1:n.918+11A=
ENST00000682811.1:c.*56+11A= ENSP00000508196.1:n.*56+11A=
ENST00000682883.1:n.1032-156A=
ENST00000682946.1:c.*87+11A= ENSP00000506856.1:n.*87+11A=
ENST00000683143.1:c.*710+11A= ENSP00000507168.1:n.*710+11A=
ENST00000683373.1:n.1510+11A=
ENST00000683558.1:n.1521A=
ENST00000683567.1:n.1114+11A=
ENST00000683955.1:n.1761+11A=
ENST00000684142.1:c.*691A= ENSP00000508008.1:n.*691A=
ENST00000684252.1:n.1413A=
ENST00000684255.1:c.*721A= ENSP00000507398.1:n.*721A=
ENST00000684315.1:n.1738+11A=
ENST00000684345.1:c.*994A= ENSP00000507163.1:n.*994A=
ENST00000684499.1:c.*1121A= ENSP00000506800.1:n.*1121A=
ENST00000684682.1:c.*747A= ENSP00000507326.1:n.*747A=
ENST00000354202.9:c.1005+11A= MANE Select ENSP00000346142.4:n.1005+11A=
ENST00000636404.1:c.233-390A=
ENST00000638850.1:c.520A=
ENST00000639704.1:c.912+11A= ENSP00000491336.1:n.912+11A=
ENST00000640102.1:c.*658+11A= ENSP00000492027.1:n.*658+11A=
ENST00000640747.1:c.*680+11A= ENSP00000492730.1:n.*680+11A=
ENST00000354202.8:c.1005+11A= ENSP00000346142.4:n.1005+11A=
ENST00000392834.7:c.*710+11A= ENSP00000376579.3:n.*710+11A=
ENST00000409993.6:c.1005+11A= ENSP00000386597.2:n.1005+11A=
ENST00000414373.5:c.*475-156A= ENSP00000402019.1:n.*475-156A=
ENST00000442480.1:c.737+11A= ENSP00000406591.1:n.737+11A=
ENST00000461999.1:n.1183A=
ENST00000481084.5:n.1634+11A=
ENST00000524658.1:n.321A=
ENST00000525456.5:n.830A=
NM_001382.3:c.1005+11A= NP_001373.2:n.1005+11A=
XM_005271422.2:c.1005+11A= XP_005271479.1:n.1005+11A=
XM_011542648.1:c.684+11A= XP_011540950.1:n.684+11A=
XR_947801.1:n.1165-156A=
XM_005271422.3:c.1005+11A= XP_005271479.1:n.1005+11A=
XM_011542648.2:c.684+11A= XP_011540950.1:n.684+11A=
XM_017017293.2:c.684+11A= XP_016872782.1:n.684+11A=
XM_017017294.2:c.*98A= XP_016872783.1:n.*98A=
XM_017017295.1:c.489+11A= XP_016872784.1:n.489+11A=
XR_001747785.2:n.1039+11A=
XR_947801.2:n.952-156A=
NM_001382.4:c.1005+11A= MANE Select NP_001373.2:n.1005+11A=