Canonical Allele Identifier: CA2003808833
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097497C= , CM000673.2:g.119097497C= GRCh38
NC_000011.9:g.118968207C= , CM000673.1:g.118968207C= GRCh37
NC_000011.8:g.118473417C= NCBI36
NG_008918.1:g.9579G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.1030G=
ENST00000524658.2:n.1011G=
ENST00000530052.2:n.2017G=
ENST00000682191.1:n.1477G=
ENST00000682192.1:n.1174G=
ENST00000682232.1:c.*623-200G= ENSP00000507302.1:n.*623-200G=
ENST00000682326.1:c.918-200G= ENSP00000508129.1:n.918-200G=
ENST00000682404.1:n.2073G=
ENST00000682517.1:n.2376G=
ENST00000682652.1:n.2246G=
ENST00000682665.1:n.1672G=
ENST00000682691.1:n.1672G=
ENST00000682791.1:c.885G= ENSP00000507312.1:p.Lys295=
ENST00000682811.1:c.*23G= ENSP00000508196.1:n.*23G=
ENST00000682883.1:n.1032-200G=
ENST00000682946.1:c.*54G= ENSP00000506856.1:n.*54G=
ENST00000683143.1:c.*677G= ENSP00000507168.1:n.*677G=
ENST00000683373.1:n.1477G=
ENST00000683558.1:n.1477G=
ENST00000683567.1:n.1081G=
ENST00000683955.1:n.1728G=
ENST00000684142.1:c.*647G= ENSP00000508008.1:n.*647G=
ENST00000684252.1:n.1369G=
ENST00000684255.1:c.*677G= ENSP00000507398.1:n.*677G=
ENST00000684315.1:n.1705G=
ENST00000684345.1:c.*950G= ENSP00000507163.1:n.*950G=
ENST00000684499.1:c.*1077G= ENSP00000506800.1:n.*1077G=
ENST00000684682.1:c.*703G= ENSP00000507326.1:n.*703G=
ENST00000354202.9:c.972G= MANE Select ENSP00000346142.4:p.Lys324=
ENST00000636404.1:c.233-434G=
ENST00000638850.1:c.476G=
ENST00000639704.1:c.879G= ENSP00000491336.1:p.Lys293=
ENST00000640102.1:c.*625G= ENSP00000492027.1:n.*625G=
ENST00000640747.1:c.*647G= ENSP00000492730.1:n.*647G=
ENST00000354202.8:c.972G= ENSP00000346142.4:p.Lys324=
ENST00000392834.7:c.*677G= ENSP00000376579.3:n.*677G=
ENST00000409993.6:c.972G= ENSP00000386597.2:p.Lys324=
ENST00000414373.5:c.*475-200G= ENSP00000402019.1:n.*475-200G=
ENST00000442480.1:c.704G= ENSP00000406591.1:n.704G=
ENST00000461999.1:n.1139G=
ENST00000481084.5:n.1601G=
ENST00000524658.1:n.277G=
ENST00000525456.5:n.786G=
NM_001382.3:c.972G= NP_001373.2:p.Lys324=
XM_005271422.2:c.972G= XP_005271479.1:p.Lys324=
XM_011542648.1:c.651G= XP_011540950.1:p.Lys217=
XR_947801.1:n.1165-200G=
XM_005271422.3:c.972G= XP_005271479.1:p.Lys324=
XM_011542648.2:c.651G= XP_011540950.1:p.Lys217=
XM_017017293.2:c.651G= XP_016872782.1:p.Lys217=
XM_017017294.2:c.*54G= XP_016872783.1:n.*54G=
XM_017017295.1:c.456G= XP_016872784.1:p.Lys152=
XR_001747785.2:n.1006G=
XR_947801.2:n.952-200G=
NM_001382.4:c.972G= MANE Select NP_001373.2:p.Lys324=