Canonical Allele Identifier: CA1339784338
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767792G= , CM000664.2:g.241767792G= GRCh38
NC_000002.11:g.242707207G= , CM000664.1:g.242707207G= GRCh37
NC_000002.10:g.242355880G= NCBI36
NG_012012.1:g.38178G=

Transcript Alleles

HGVS Amino-acid change
ENST00000321264.9:c.1389G= MANE Select ENSP00000315351.4:p.Glu463=
ENST00000321264.8:c.1389G= ENSP00000315351.4:p.Glu463=
ENST00000400769.6:c.*139G= ENSP00000383580.2:n.*139G=
ENST00000403782.5:c.987G= ENSP00000384723.1:p.Glu329=
ENST00000436747.5:c.*2625G= ENSP00000400212.1:n.*2625G=
ENST00000445308.1:c.785G=
ENST00000468064.5:n.1279G=
ENST00000470343.5:n.870G=
ENST00000473126.1:n.588G=
ENST00000486953.5:n.1213G=
ENST00000610344.1:c.*233G= ENSP00000481906.1:n.*233G=
NM_001287249.1:c.987G= NP_001274178.1:p.Glu329=
NM_152783.4:c.1389G= NP_689996.4:p.Glu463=
NR_109778.1:n.1311G=
XM_011511734.1:c.1509G= XP_011510036.1:p.Glu503=
XM_011511735.1:c.1467G= XP_011510037.1:p.Glu489=
XM_011511736.1:c.1431G= XP_011510038.1:p.Glu477=
XM_011511744.1:c.*121G= XP_011510046.1:n.*121G=
XM_011511750.1:c.*56G= XP_011510052.1:n.*56G=
XM_011511754.1:c.948G= XP_011510056.1:p.Glu316=
XM_011511755.1:c.939G= XP_011510057.1:p.Glu313=
XM_011511756.1:c.936G= XP_011510058.1:p.Glu312=
XR_923004.1:n.2021G=
XR_923007.1:n.1731G=
XR_923011.1:n.1832G=
NM_001352824.1:c.828G= NP_001339753.1:p.Glu276=
XM_011511734.2:c.1509G= XP_011510036.1:p.Glu503=
XM_011511735.2:c.1467G= XP_011510037.1:p.Glu489=
XM_011511736.2:c.1431G= XP_011510038.1:p.Glu477=
XM_011511750.3:c.*56G= XP_011510052.1:n.*56G=
XM_011511756.2:c.936G= XP_011510058.1:p.Glu312=
XM_024453102.1:c.1281G= XP_024308870.1:p.Glu427=
XR_001738918.2:n.1763G=
XR_001738919.2:n.1697G=
XR_923004.3:n.2020G=
XR_923007.3:n.1730G=
XR_923011.3:n.1831G=
NM_152783.5:c.1389G= MANE Select NP_689996.4:p.Glu463=
NM_001287249.2:c.987G= NP_001274178.1:p.Glu329=
NM_001352824.2:c.828G= NP_001339753.1:p.Glu276=
NR_109778.2:n.1260G=