Canonical Allele Identifier: CA2003810069
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119100396T= , CM000673.2:g.119100396T= GRCh38
NC_000011.9:g.118971106T= , CM000673.1:g.118971106T= GRCh37
NC_000011.8:g.118476316T= NCBI36
NG_008918.1:g.6680A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.685A=
ENST00000530052.2:n.1251A=
ENST00000682191.1:n.711A=
ENST00000682192.1:n.711A=
ENST00000682232.1:c.*214A= ENSP00000507302.1:n.*214A=
ENST00000682326.1:c.509A= ENSP00000508129.1:p.Tyr170=
ENST00000682404.1:n.1251A=
ENST00000682517.1:n.1251A=
ENST00000682652.1:n.1480A=
ENST00000682665.1:n.906A=
ENST00000682691.1:n.906A=
ENST00000682791.1:c.422A= ENSP00000507312.1:p.Tyr141=
ENST00000682811.1:c.509A= ENSP00000508196.1:p.Tyr170=
ENST00000682883.1:n.812A=
ENST00000682946.1:c.509A= ENSP00000506856.1:p.Tyr170=
ENST00000683143.1:c.*214A= ENSP00000507168.1:n.*214A=
ENST00000683373.1:n.711A=
ENST00000683558.1:n.711A=
ENST00000683567.1:n.736A=
ENST00000683955.1:n.906A=
ENST00000684142.1:c.*184A= ENSP00000508008.1:n.*184A=
ENST00000684252.1:n.906A=
ENST00000684255.1:c.*214A= ENSP00000507398.1:n.*214A=
ENST00000684315.1:n.1242A=
ENST00000684345.1:c.*184A= ENSP00000507163.1:n.*184A=
ENST00000684499.1:c.*614A= ENSP00000506800.1:n.*614A=
ENST00000684682.1:c.174A= ENSP00000507326.1:p.Leu58=
ENST00000354202.9:c.509A= MANE Select ENSP00000346142.4:p.Tyr170=
ENST00000636404.1:c.13A=
ENST00000638850.1:c.13A=
ENST00000639704.1:c.416A= ENSP00000491336.1:p.Tyr139=
ENST00000640102.1:c.*162A= ENSP00000492027.1:n.*162A=
ENST00000640747.1:c.*184A= ENSP00000492730.1:n.*184A=
ENST00000354202.8:c.509A= ENSP00000346142.4:p.Tyr170=
ENST00000392834.7:c.*214A= ENSP00000376579.3:n.*214A=
ENST00000409993.6:c.509A= ENSP00000386597.2:p.Tyr170=
ENST00000414373.5:c.*255A= ENSP00000402019.1:n.*255A=
ENST00000442480.1:c.359A= ENSP00000406591.1:p.Tyr120=
ENST00000461999.1:n.14A=
ENST00000481084.5:n.1138A=
ENST00000525456.5:n.512A=
ENST00000530052.1:n.407A=
ENST00000533687.1:n.521A=
NM_001382.3:c.509A= NP_001373.2:p.Tyr170=
XM_005271422.2:c.509A= XP_005271479.1:p.Tyr170=
XM_011542648.1:c.188A= XP_011540950.1:p.Tyr63=
XR_947801.1:n.945A=
XM_005271422.3:c.509A= XP_005271479.1:p.Tyr170=
XM_011542648.2:c.188A= XP_011540950.1:p.Tyr63=
XM_017017293.2:c.188A= XP_016872782.1:p.Tyr63=
XM_017017294.2:c.509A= XP_016872783.1:p.Tyr170=
XM_017017295.1:c.-8A= XP_016872784.1:n.-8A=
XR_001747785.2:n.732A=
XR_947801.2:n.732A=
NM_001382.4:c.509A= MANE Select NP_001373.2:p.Tyr170=