Canonical Allele Identifier: CA2003808900
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097661T= , CM000673.2:g.119097661T= GRCh38
NC_000011.9:g.118968371T= , CM000673.1:g.118968371T= GRCh37
NC_000011.8:g.118473581T= NCBI36
NG_008918.1:g.9415A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.976-110A=
ENST00000524658.2:n.957-110A=
ENST00000530052.2:n.1853A=
ENST00000682191.1:n.1313A=
ENST00000682192.1:n.1120-110A=
ENST00000682232.1:c.*622+194A= ENSP00000507302.1:n.*622+194A=
ENST00000682326.1:c.917+194A= ENSP00000508129.1:n.917+194A=
ENST00000682404.1:n.2019-110A=
ENST00000682517.1:n.2212A=
ENST00000682652.1:n.2082A=
ENST00000682665.1:n.1508A=
ENST00000682691.1:n.1508A=
ENST00000682791.1:c.831-110A= ENSP00000507312.1:n.831-110A=
ENST00000682811.1:c.800-110A= ENSP00000508196.1:n.800-110A=
ENST00000682883.1:n.1032-364A=
ENST00000682946.1:c.729-110A= ENSP00000506856.1:n.729-110A=
ENST00000683143.1:c.*623-110A= ENSP00000507168.1:n.*623-110A=
ENST00000683373.1:n.1313A=
ENST00000683558.1:n.1313A=
ENST00000683567.1:n.1027-110A=
ENST00000683955.1:n.1674-110A=
ENST00000684142.1:c.*593-110A= ENSP00000508008.1:n.*593-110A=
ENST00000684252.1:n.1315-110A=
ENST00000684255.1:c.*623-110A= ENSP00000507398.1:n.*623-110A=
ENST00000684315.1:n.1651-110A=
ENST00000684345.1:c.*786A= ENSP00000507163.1:n.*786A=
ENST00000684499.1:c.*1023-110A= ENSP00000506800.1:n.*1023-110A=
ENST00000684682.1:c.*539A= ENSP00000507326.1:n.*539A=
ENST00000354202.9:c.918-110A= MANE Select ENSP00000346142.4:n.918-110A=
ENST00000636404.1:c.233-598A=
ENST00000638850.1:c.422-110A=
ENST00000639704.1:c.825-110A= ENSP00000491336.1:n.825-110A=
ENST00000640102.1:c.*571-110A= ENSP00000492027.1:n.*571-110A=
ENST00000640747.1:c.*593-110A= ENSP00000492730.1:n.*593-110A=
ENST00000354202.8:c.918-110A= ENSP00000346142.4:n.918-110A=
ENST00000392834.7:c.*623-110A= ENSP00000376579.3:n.*623-110A=
ENST00000409993.6:c.918-110A= ENSP00000386597.2:n.918-110A=
ENST00000414373.5:c.*475-364A= ENSP00000402019.1:n.*475-364A=
ENST00000442480.1:c.650-110A= ENSP00000406591.1:n.650-110A=
ENST00000461999.1:n.975A=
ENST00000481084.5:n.1547-110A=
ENST00000524658.1:n.223-110A=
ENST00000525456.5:n.732-110A=
NM_001382.3:c.918-110A= NP_001373.2:n.918-110A=
XM_005271422.2:c.918-110A= XP_005271479.1:n.918-110A=
XM_011542648.1:c.597-110A= XP_011540950.1:n.597-110A=
XR_947801.1:n.1165-364A=
XM_005271422.3:c.918-110A= XP_005271479.1:n.918-110A=
XM_011542648.2:c.597-110A= XP_011540950.1:n.597-110A=
XM_017017293.2:c.597-110A= XP_016872782.1:n.597-110A=
XM_017017294.2:c.729-110A= XP_016872783.1:n.729-110A=
XM_017017295.1:c.402-110A= XP_016872784.1:n.402-110A=
XR_001747785.2:n.952-110A=
XR_947801.2:n.952-364A=
NM_001382.4:c.918-110A= MANE Select NP_001373.2:n.918-110A=