Canonical Allele Identifier: CA2003808818
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097472T= , CM000673.2:g.119097472T= GRCh38
NC_000011.9:g.118968182T= , CM000673.1:g.118968182T= GRCh37
NC_000011.8:g.118473392T= NCBI36
NG_008918.1:g.9604A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.1055A=
ENST00000524658.2:n.1036A=
ENST00000530052.2:n.2042A=
ENST00000682191.1:n.1502A=
ENST00000682192.1:n.1199A=
ENST00000682232.1:c.*623-175A= ENSP00000507302.1:n.*623-175A=
ENST00000682326.1:c.918-175A= ENSP00000508129.1:n.918-175A=
ENST00000682404.1:n.2098A=
ENST00000682517.1:n.2401A=
ENST00000682652.1:n.2271A=
ENST00000682665.1:n.1697A=
ENST00000682691.1:n.1697A=
ENST00000682791.1:c.910A= ENSP00000507312.1:p.Ile304=
ENST00000682811.1:c.*48A= ENSP00000508196.1:n.*48A=
ENST00000682883.1:n.1032-175A=
ENST00000682946.1:c.*79A= ENSP00000506856.1:n.*79A=
ENST00000683143.1:c.*702A= ENSP00000507168.1:n.*702A=
ENST00000683373.1:n.1502A=
ENST00000683558.1:n.1502A=
ENST00000683567.1:n.1106A=
ENST00000683955.1:n.1753A=
ENST00000684142.1:c.*672A= ENSP00000508008.1:n.*672A=
ENST00000684252.1:n.1394A=
ENST00000684255.1:c.*702A= ENSP00000507398.1:n.*702A=
ENST00000684315.1:n.1730A=
ENST00000684345.1:c.*975A= ENSP00000507163.1:n.*975A=
ENST00000684499.1:c.*1102A= ENSP00000506800.1:n.*1102A=
ENST00000684682.1:c.*728A= ENSP00000507326.1:n.*728A=
ENST00000354202.9:c.997A= MANE Select ENSP00000346142.4:p.Ile333=
ENST00000636404.1:c.233-409A=
ENST00000638850.1:c.501A=
ENST00000639704.1:c.904A= ENSP00000491336.1:p.Ile302=
ENST00000640102.1:c.*650A= ENSP00000492027.1:n.*650A=
ENST00000640747.1:c.*672A= ENSP00000492730.1:n.*672A=
ENST00000354202.8:c.997A= ENSP00000346142.4:p.Ile333=
ENST00000392834.7:c.*702A= ENSP00000376579.3:n.*702A=
ENST00000409993.6:c.997A= ENSP00000386597.2:p.Ile333=
ENST00000414373.5:c.*475-175A= ENSP00000402019.1:n.*475-175A=
ENST00000442480.1:c.729A= ENSP00000406591.1:n.729A=
ENST00000461999.1:n.1164A=
ENST00000481084.5:n.1626A=
ENST00000524658.1:n.302A=
ENST00000525456.5:n.811A=
NM_001382.3:c.997A= NP_001373.2:p.Ile333=
XM_005271422.2:c.997A= XP_005271479.1:p.Ile333=
XM_011542648.1:c.676A= XP_011540950.1:p.Ile226=
XR_947801.1:n.1165-175A=
XM_005271422.3:c.997A= XP_005271479.1:p.Ile333=
XM_011542648.2:c.676A= XP_011540950.1:p.Ile226=
XM_017017293.2:c.676A= XP_016872782.1:p.Ile226=
XM_017017294.2:c.*79A= XP_016872783.1:n.*79A=
XM_017017295.1:c.481A= XP_016872784.1:p.Ile161=
XR_001747785.2:n.1031A=
XR_947801.2:n.952-175A=
NM_001382.4:c.997A= MANE Select NP_001373.2:p.Ile333=