Canonical Allele Identifier: CA2003808788
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097394A= , CM000673.2:g.119097394A= GRCh38
NC_000011.9:g.118968104A= , CM000673.1:g.118968104A= GRCh37
NC_000011.8:g.118473314A= NCBI36
NG_008918.1:g.9682T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.1133T=
ENST00000524658.2:n.1114T=
ENST00000530052.2:n.2120T=
ENST00000682191.1:n.1510+70T=
ENST00000682192.1:n.1277T=
ENST00000682232.1:c.*623-97T= ENSP00000507302.1:n.*623-97T=
ENST00000682326.1:c.918-97T= ENSP00000508129.1:n.918-97T=
ENST00000682404.1:n.2176T=
ENST00000682517.1:n.2479T=
ENST00000682652.1:n.2279+70T=
ENST00000682665.1:n.1775T=
ENST00000682691.1:n.1775T=
ENST00000682791.1:c.918+70T= ENSP00000507312.1:n.918+70T=
ENST00000682811.1:c.*56+70T= ENSP00000508196.1:n.*56+70T=
ENST00000682883.1:n.1032-97T=
ENST00000682946.1:c.*87+70T= ENSP00000506856.1:n.*87+70T=
ENST00000683143.1:c.*710+70T= ENSP00000507168.1:n.*710+70T=
ENST00000683373.1:n.1510+70T=
ENST00000683558.1:n.1580T=
ENST00000683567.1:n.1114+70T=
ENST00000683955.1:n.1761+70T=
ENST00000684142.1:c.*750T= ENSP00000508008.1:n.*750T=
ENST00000684252.1:n.1472T=
ENST00000684255.1:c.*780T= ENSP00000507398.1:n.*780T=
ENST00000684315.1:n.1738+70T=
ENST00000684345.1:c.*1053T= ENSP00000507163.1:n.*1053T=
ENST00000684499.1:c.*1180T= ENSP00000506800.1:n.*1180T=
ENST00000684682.1:c.*806T= ENSP00000507326.1:n.*806T=
ENST00000354202.9:c.1005+70T= MANE Select ENSP00000346142.4:n.1005+70T=
ENST00000636404.1:c.233-331T=
ENST00000638850.1:c.528+51T=
ENST00000639704.1:c.912+70T= ENSP00000491336.1:n.912+70T=
ENST00000640102.1:c.*658+70T= ENSP00000492027.1:n.*658+70T=
ENST00000640747.1:c.*680+70T= ENSP00000492730.1:n.*680+70T=
ENST00000354202.8:c.1005+70T= ENSP00000346142.4:n.1005+70T=
ENST00000392834.7:c.*710+70T= ENSP00000376579.3:n.*710+70T=
ENST00000409993.6:c.1005+70T= ENSP00000386597.2:n.1005+70T=
ENST00000414373.5:c.*475-97T= ENSP00000402019.1:n.*475-97T=
ENST00000442480.1:c.737+70T= ENSP00000406591.1:n.737+70T=
ENST00000461999.1:n.1242T=
ENST00000481084.5:n.1634+70T=
ENST00000524658.1:n.380T=
ENST00000525456.5:n.889T=
NM_001382.3:c.1005+70T= NP_001373.2:n.1005+70T=
XM_005271422.2:c.1005+70T= XP_005271479.1:n.1005+70T=
XM_011542648.1:c.684+70T= XP_011540950.1:n.684+70T=
XR_947801.1:n.1165-97T=
XM_005271422.3:c.1005+70T= XP_005271479.1:n.1005+70T=
XM_011542648.2:c.684+70T= XP_011540950.1:n.684+70T=
XM_017017293.2:c.684+70T= XP_016872782.1:n.684+70T=
XM_017017294.2:c.*157T= XP_016872783.1:n.*157T=
XM_017017295.1:c.489+70T= XP_016872784.1:n.489+70T=
XR_001747785.2:n.1039+70T=
XR_947801.2:n.952-97T=
NM_001382.4:c.1005+70T= MANE Select NP_001373.2:n.1005+70T=