Canonical Allele Identifier: CA2003808802
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097418G= , CM000673.2:g.119097418G= GRCh38
NC_000011.9:g.118968128G= , CM000673.1:g.118968128G= GRCh37
NC_000011.8:g.118473338G= NCBI36
NG_008918.1:g.9658C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.1109C=
ENST00000524658.2:n.1090C=
ENST00000530052.2:n.2096C=
ENST00000682191.1:n.1510+46C=
ENST00000682192.1:n.1253C=
ENST00000682232.1:c.*623-121C= ENSP00000507302.1:n.*623-121C=
ENST00000682326.1:c.918-121C= ENSP00000508129.1:n.918-121C=
ENST00000682404.1:n.2152C=
ENST00000682517.1:n.2455C=
ENST00000682652.1:n.2279+46C=
ENST00000682665.1:n.1751C=
ENST00000682691.1:n.1751C=
ENST00000682791.1:c.918+46C= ENSP00000507312.1:n.918+46C=
ENST00000682811.1:c.*56+46C= ENSP00000508196.1:n.*56+46C=
ENST00000682883.1:n.1032-121C=
ENST00000682946.1:c.*87+46C= ENSP00000506856.1:n.*87+46C=
ENST00000683143.1:c.*710+46C= ENSP00000507168.1:n.*710+46C=
ENST00000683373.1:n.1510+46C=
ENST00000683558.1:n.1556C=
ENST00000683567.1:n.1114+46C=
ENST00000683955.1:n.1761+46C=
ENST00000684142.1:c.*726C= ENSP00000508008.1:n.*726C=
ENST00000684252.1:n.1448C=
ENST00000684255.1:c.*756C= ENSP00000507398.1:n.*756C=
ENST00000684315.1:n.1738+46C=
ENST00000684345.1:c.*1029C= ENSP00000507163.1:n.*1029C=
ENST00000684499.1:c.*1156C= ENSP00000506800.1:n.*1156C=
ENST00000684682.1:c.*782C= ENSP00000507326.1:n.*782C=
ENST00000354202.9:c.1005+46C= MANE Select ENSP00000346142.4:n.1005+46C=
ENST00000636404.1:c.233-355C=
ENST00000638850.1:c.528+27C=
ENST00000639704.1:c.912+46C= ENSP00000491336.1:n.912+46C=
ENST00000640102.1:c.*658+46C= ENSP00000492027.1:n.*658+46C=
ENST00000640747.1:c.*680+46C= ENSP00000492730.1:n.*680+46C=
ENST00000354202.8:c.1005+46C= ENSP00000346142.4:n.1005+46C=
ENST00000392834.7:c.*710+46C= ENSP00000376579.3:n.*710+46C=
ENST00000409993.6:c.1005+46C= ENSP00000386597.2:n.1005+46C=
ENST00000414373.5:c.*475-121C= ENSP00000402019.1:n.*475-121C=
ENST00000442480.1:c.737+46C= ENSP00000406591.1:n.737+46C=
ENST00000461999.1:n.1218C=
ENST00000481084.5:n.1634+46C=
ENST00000524658.1:n.356C=
ENST00000525456.5:n.865C=
NM_001382.3:c.1005+46C= NP_001373.2:n.1005+46C=
XM_005271422.2:c.1005+46C= XP_005271479.1:n.1005+46C=
XM_011542648.1:c.684+46C= XP_011540950.1:n.684+46C=
XR_947801.1:n.1165-121C=
XM_005271422.3:c.1005+46C= XP_005271479.1:n.1005+46C=
XM_011542648.2:c.684+46C= XP_011540950.1:n.684+46C=
XM_017017293.2:c.684+46C= XP_016872782.1:n.684+46C=
XM_017017294.2:c.*133C= XP_016872783.1:n.*133C=
XM_017017295.1:c.489+46C= XP_016872784.1:n.489+46C=
XR_001747785.2:n.1039+46C=
XR_947801.2:n.952-121C=
NM_001382.4:c.1005+46C= MANE Select NP_001373.2:n.1005+46C=