Canonical Allele Identifier: CA2003808825
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097480C= , CM000673.2:g.119097480C= GRCh38
NC_000011.9:g.118968190C= , CM000673.1:g.118968190C= GRCh37
NC_000011.8:g.118473400C= NCBI36
NG_008918.1:g.9596G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.1047G=
ENST00000524658.2:n.1028G=
ENST00000530052.2:n.2034G=
ENST00000682191.1:n.1494G=
ENST00000682192.1:n.1191G=
ENST00000682232.1:c.*623-183G= ENSP00000507302.1:n.*623-183G=
ENST00000682326.1:c.918-183G= ENSP00000508129.1:n.918-183G=
ENST00000682404.1:n.2090G=
ENST00000682517.1:n.2393G=
ENST00000682652.1:n.2263G=
ENST00000682665.1:n.1689G=
ENST00000682691.1:n.1689G=
ENST00000682791.1:c.902G= ENSP00000507312.1:p.Gly301=
ENST00000682811.1:c.*40G= ENSP00000508196.1:n.*40G=
ENST00000682883.1:n.1032-183G=
ENST00000682946.1:c.*71G= ENSP00000506856.1:n.*71G=
ENST00000683143.1:c.*694G= ENSP00000507168.1:n.*694G=
ENST00000683373.1:n.1494G=
ENST00000683558.1:n.1494G=
ENST00000683567.1:n.1098G=
ENST00000683955.1:n.1745G=
ENST00000684142.1:c.*664G= ENSP00000508008.1:n.*664G=
ENST00000684252.1:n.1386G=
ENST00000684255.1:c.*694G= ENSP00000507398.1:n.*694G=
ENST00000684315.1:n.1722G=
ENST00000684345.1:c.*967G= ENSP00000507163.1:n.*967G=
ENST00000684499.1:c.*1094G= ENSP00000506800.1:n.*1094G=
ENST00000684682.1:c.*720G= ENSP00000507326.1:n.*720G=
ENST00000354202.9:c.989G= MANE Select ENSP00000346142.4:p.Gly330=
ENST00000636404.1:c.233-417G=
ENST00000638850.1:c.493G=
ENST00000639704.1:c.896G= ENSP00000491336.1:p.Gly299=
ENST00000640102.1:c.*642G= ENSP00000492027.1:n.*642G=
ENST00000640747.1:c.*664G= ENSP00000492730.1:n.*664G=
ENST00000354202.8:c.989G= ENSP00000346142.4:p.Gly330=
ENST00000392834.7:c.*694G= ENSP00000376579.3:n.*694G=
ENST00000409993.6:c.989G= ENSP00000386597.2:p.Gly330=
ENST00000414373.5:c.*475-183G= ENSP00000402019.1:n.*475-183G=
ENST00000442480.1:c.721G= ENSP00000406591.1:n.721G=
ENST00000461999.1:n.1156G=
ENST00000481084.5:n.1618G=
ENST00000524658.1:n.294G=
ENST00000525456.5:n.803G=
NM_001382.3:c.989G= NP_001373.2:p.Gly330=
XM_005271422.2:c.989G= XP_005271479.1:p.Gly330=
XM_011542648.1:c.668G= XP_011540950.1:p.Gly223=
XR_947801.1:n.1165-183G=
XM_005271422.3:c.989G= XP_005271479.1:p.Gly330=
XM_011542648.2:c.668G= XP_011540950.1:p.Gly223=
XM_017017293.2:c.668G= XP_016872782.1:p.Gly223=
XM_017017294.2:c.*71G= XP_016872783.1:n.*71G=
XM_017017295.1:c.473G= XP_016872784.1:p.Gly158=
XR_001747785.2:n.1023G=
XR_947801.2:n.952-183G=
NM_001382.4:c.989G= MANE Select NP_001373.2:p.Gly330=