Canonical Allele Identifier: CA2003808829
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097491G= , CM000673.2:g.119097491G= GRCh38
NC_000011.9:g.118968201G= , CM000673.1:g.118968201G= GRCh37
NC_000011.8:g.118473411G= NCBI36
NG_008918.1:g.9585C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.1036C=
ENST00000524658.2:n.1017C=
ENST00000530052.2:n.2023C=
ENST00000682191.1:n.1483C=
ENST00000682192.1:n.1180C=
ENST00000682232.1:c.*623-194C= ENSP00000507302.1:n.*623-194C=
ENST00000682326.1:c.918-194C= ENSP00000508129.1:n.918-194C=
ENST00000682404.1:n.2079C=
ENST00000682517.1:n.2382C=
ENST00000682652.1:n.2252C=
ENST00000682665.1:n.1678C=
ENST00000682691.1:n.1678C=
ENST00000682791.1:c.891C= ENSP00000507312.1:p.Leu297=
ENST00000682811.1:c.*29C= ENSP00000508196.1:n.*29C=
ENST00000682883.1:n.1032-194C=
ENST00000682946.1:c.*60C= ENSP00000506856.1:n.*60C=
ENST00000683143.1:c.*683C= ENSP00000507168.1:n.*683C=
ENST00000683373.1:n.1483C=
ENST00000683558.1:n.1483C=
ENST00000683567.1:n.1087C=
ENST00000683955.1:n.1734C=
ENST00000684142.1:c.*653C= ENSP00000508008.1:n.*653C=
ENST00000684252.1:n.1375C=
ENST00000684255.1:c.*683C= ENSP00000507398.1:n.*683C=
ENST00000684315.1:n.1711C=
ENST00000684345.1:c.*956C= ENSP00000507163.1:n.*956C=
ENST00000684499.1:c.*1083C= ENSP00000506800.1:n.*1083C=
ENST00000684682.1:c.*709C= ENSP00000507326.1:n.*709C=
ENST00000354202.9:c.978C= MANE Select ENSP00000346142.4:p.Leu326=
ENST00000636404.1:c.233-428C=
ENST00000638850.1:c.482C=
ENST00000639704.1:c.885C= ENSP00000491336.1:p.Leu295=
ENST00000640102.1:c.*631C= ENSP00000492027.1:n.*631C=
ENST00000640747.1:c.*653C= ENSP00000492730.1:n.*653C=
ENST00000354202.8:c.978C= ENSP00000346142.4:p.Leu326=
ENST00000392834.7:c.*683C= ENSP00000376579.3:n.*683C=
ENST00000409993.6:c.978C= ENSP00000386597.2:p.Leu326=
ENST00000414373.5:c.*475-194C= ENSP00000402019.1:n.*475-194C=
ENST00000442480.1:c.710C= ENSP00000406591.1:n.710C=
ENST00000461999.1:n.1145C=
ENST00000481084.5:n.1607C=
ENST00000524658.1:n.283C=
ENST00000525456.5:n.792C=
NM_001382.3:c.978C= NP_001373.2:p.Leu326=
XM_005271422.2:c.978C= XP_005271479.1:p.Leu326=
XM_011542648.1:c.657C= XP_011540950.1:p.Leu219=
XR_947801.1:n.1165-194C=
XM_005271422.3:c.978C= XP_005271479.1:p.Leu326=
XM_011542648.2:c.657C= XP_011540950.1:p.Leu219=
XM_017017293.2:c.657C= XP_016872782.1:p.Leu219=
XM_017017294.2:c.*60C= XP_016872783.1:n.*60C=
XM_017017295.1:c.462C= XP_016872784.1:p.Leu154=
XR_001747785.2:n.1012C=
XR_947801.2:n.952-194C=
NM_001382.4:c.978C= MANE Select NP_001373.2:p.Leu326=