Canonical Allele Identifier: CA2003808848
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097546T= , CM000673.2:g.119097546T= GRCh38
NC_000011.9:g.118968256T= , CM000673.1:g.118968256T= GRCh37
NC_000011.8:g.118473466T= NCBI36
NG_008918.1:g.9530A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.981A=
ENST00000524658.2:n.962A=
ENST00000530052.2:n.1968A=
ENST00000682191.1:n.1428A=
ENST00000682192.1:n.1125A=
ENST00000682232.1:c.*623-249A= ENSP00000507302.1:n.*623-249A=
ENST00000682326.1:c.918-249A= ENSP00000508129.1:n.918-249A=
ENST00000682404.1:n.2024A=
ENST00000682517.1:n.2327A=
ENST00000682652.1:n.2197A=
ENST00000682665.1:n.1623A=
ENST00000682691.1:n.1623A=
ENST00000682791.1:c.836A= ENSP00000507312.1:p.Asn279=
ENST00000682811.1:c.805A= ENSP00000508196.1:p.Ile269=
ENST00000682883.1:n.1032-249A=
ENST00000682946.1:c.*5A= ENSP00000506856.1:n.*5A=
ENST00000683143.1:c.*628A= ENSP00000507168.1:n.*628A=
ENST00000683373.1:n.1428A=
ENST00000683558.1:n.1428A=
ENST00000683567.1:n.1032A=
ENST00000683955.1:n.1679A=
ENST00000684142.1:c.*598A= ENSP00000508008.1:n.*598A=
ENST00000684252.1:n.1320A=
ENST00000684255.1:c.*628A= ENSP00000507398.1:n.*628A=
ENST00000684315.1:n.1656A=
ENST00000684345.1:c.*901A= ENSP00000507163.1:n.*901A=
ENST00000684499.1:c.*1028A= ENSP00000506800.1:n.*1028A=
ENST00000684682.1:c.*654A= ENSP00000507326.1:n.*654A=
ENST00000354202.9:c.923A= MANE Select ENSP00000346142.4:p.Asn308=
ENST00000636404.1:c.233-483A=
ENST00000638850.1:c.427A=
ENST00000639704.1:c.830A= ENSP00000491336.1:p.Asn277=
ENST00000640102.1:c.*576A= ENSP00000492027.1:n.*576A=
ENST00000640747.1:c.*598A= ENSP00000492730.1:n.*598A=
ENST00000354202.8:c.923A= ENSP00000346142.4:p.Asn308=
ENST00000392834.7:c.*628A= ENSP00000376579.3:n.*628A=
ENST00000409993.6:c.923A= ENSP00000386597.2:p.Asn308=
ENST00000414373.5:c.*475-249A= ENSP00000402019.1:n.*475-249A=
ENST00000442480.1:c.655A= ENSP00000406591.1:p.Ile219=
ENST00000461999.1:n.1090A=
ENST00000481084.5:n.1552A=
ENST00000524658.1:n.228A=
ENST00000525456.5:n.737A=
NM_001382.3:c.923A= NP_001373.2:p.Asn308=
XM_005271422.2:c.923A= XP_005271479.1:p.Asn308=
XM_011542648.1:c.602A= XP_011540950.1:p.Asn201=
XR_947801.1:n.1165-249A=
XM_005271422.3:c.923A= XP_005271479.1:p.Asn308=
XM_011542648.2:c.602A= XP_011540950.1:p.Asn201=
XM_017017293.2:c.602A= XP_016872782.1:p.Asn201=
XM_017017294.2:c.*5A= XP_016872783.1:n.*5A=
XM_017017295.1:c.407A= XP_016872784.1:p.Asn136=
XR_001747785.2:n.957A=
XR_947801.2:n.952-249A=
NM_001382.4:c.923A= MANE Select NP_001373.2:p.Asn308=