Canonical Allele Identifier: CA2003808793
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097405C= , CM000673.2:g.119097405C= GRCh38
NC_000011.9:g.118968115C= , CM000673.1:g.118968115C= GRCh37
NC_000011.8:g.118473325C= NCBI36
NG_008918.1:g.9671G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.1122G=
ENST00000524658.2:n.1103G=
ENST00000530052.2:n.2109G=
ENST00000682191.1:n.1510+59G=
ENST00000682192.1:n.1266G=
ENST00000682232.1:c.*623-108G= ENSP00000507302.1:n.*623-108G=
ENST00000682326.1:c.918-108G= ENSP00000508129.1:n.918-108G=
ENST00000682404.1:n.2165G=
ENST00000682517.1:n.2468G=
ENST00000682652.1:n.2279+59G=
ENST00000682665.1:n.1764G=
ENST00000682691.1:n.1764G=
ENST00000682791.1:c.918+59G= ENSP00000507312.1:n.918+59G=
ENST00000682811.1:c.*56+59G= ENSP00000508196.1:n.*56+59G=
ENST00000682883.1:n.1032-108G=
ENST00000682946.1:c.*87+59G= ENSP00000506856.1:n.*87+59G=
ENST00000683143.1:c.*710+59G= ENSP00000507168.1:n.*710+59G=
ENST00000683373.1:n.1510+59G=
ENST00000683558.1:n.1569G=
ENST00000683567.1:n.1114+59G=
ENST00000683955.1:n.1761+59G=
ENST00000684142.1:c.*739G= ENSP00000508008.1:n.*739G=
ENST00000684252.1:n.1461G=
ENST00000684255.1:c.*769G= ENSP00000507398.1:n.*769G=
ENST00000684315.1:n.1738+59G=
ENST00000684345.1:c.*1042G= ENSP00000507163.1:n.*1042G=
ENST00000684499.1:c.*1169G= ENSP00000506800.1:n.*1169G=
ENST00000684682.1:c.*795G= ENSP00000507326.1:n.*795G=
ENST00000354202.9:c.1005+59G= MANE Select ENSP00000346142.4:n.1005+59G=
ENST00000636404.1:c.233-342G=
ENST00000638850.1:c.528+40G=
ENST00000639704.1:c.912+59G= ENSP00000491336.1:n.912+59G=
ENST00000640102.1:c.*658+59G= ENSP00000492027.1:n.*658+59G=
ENST00000640747.1:c.*680+59G= ENSP00000492730.1:n.*680+59G=
ENST00000354202.8:c.1005+59G= ENSP00000346142.4:n.1005+59G=
ENST00000392834.7:c.*710+59G= ENSP00000376579.3:n.*710+59G=
ENST00000409993.6:c.1005+59G= ENSP00000386597.2:n.1005+59G=
ENST00000414373.5:c.*475-108G= ENSP00000402019.1:n.*475-108G=
ENST00000442480.1:c.737+59G= ENSP00000406591.1:n.737+59G=
ENST00000461999.1:n.1231G=
ENST00000481084.5:n.1634+59G=
ENST00000524658.1:n.369G=
ENST00000525456.5:n.878G=
NM_001382.3:c.1005+59G= NP_001373.2:n.1005+59G=
XM_005271422.2:c.1005+59G= XP_005271479.1:n.1005+59G=
XM_011542648.1:c.684+59G= XP_011540950.1:n.684+59G=
XR_947801.1:n.1165-108G=
XM_005271422.3:c.1005+59G= XP_005271479.1:n.1005+59G=
XM_011542648.2:c.684+59G= XP_011540950.1:n.684+59G=
XM_017017293.2:c.684+59G= XP_016872782.1:n.684+59G=
XM_017017294.2:c.*146G= XP_016872783.1:n.*146G=
XM_017017295.1:c.489+59G= XP_016872784.1:n.489+59G=
XR_001747785.2:n.1039+59G=
XR_947801.2:n.952-108G=
NM_001382.4:c.1005+59G= MANE Select NP_001373.2:n.1005+59G=