Canonical Allele Identifier: CA1339784330
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767773T= , CM000664.2:g.241767773T= GRCh38
NC_000002.11:g.242707188T= , CM000664.1:g.242707188T= GRCh37
NC_000002.10:g.242355861T= NCBI36
NG_012012.1:g.38159T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.1370T= MANE Select ENSP00000315351.4:p.Leu457=
ENST00000321264.8:c.1370T= ENSP00000315351.4:p.Leu457=
ENST00000400769.6:c.*120T= ENSP00000383580.2:n.*120T=
ENST00000403782.5:c.968T= ENSP00000384723.1:p.Leu323=
ENST00000436747.5:c.*2606T= ENSP00000400212.1:n.*2606T=
ENST00000445308.1:c.766T=
ENST00000468064.5:n.1260T=
ENST00000470343.5:n.851T=
ENST00000473126.1:n.569T=
ENST00000486953.5:n.1194T=
ENST00000610344.1:c.*214T= ENSP00000481906.1:n.*214T=
NM_001287249.1:c.968T= NP_001274178.1:p.Leu323=
NM_152783.4:c.1370T= NP_689996.4:p.Leu457=
NR_109778.1:n.1292T=
XM_011511734.1:c.1490T= XP_011510036.1:p.Leu497=
XM_011511735.1:c.1448T= XP_011510037.1:p.Leu483=
XM_011511736.1:c.1412T= XP_011510038.1:p.Leu471=
XM_011511744.1:c.*102T= XP_011510046.1:n.*102T=
XM_011511750.1:c.*37T= XP_011510052.1:n.*37T=
XM_011511754.1:c.929T= XP_011510056.1:p.Leu310=
XM_011511755.1:c.920T= XP_011510057.1:p.Leu307=
XM_011511756.1:c.917T= XP_011510058.1:p.Leu306=
XR_923004.1:n.2002T=
XR_923007.1:n.1712T=
XR_923011.1:n.1813T=
NM_001352824.1:c.809T= NP_001339753.1:p.Leu270=
XM_011511734.2:c.1490T= XP_011510036.1:p.Leu497=
XM_011511735.2:c.1448T= XP_011510037.1:p.Leu483=
XM_011511736.2:c.1412T= XP_011510038.1:p.Leu471=
XM_011511744.2:c.*102T= XP_011510046.1:n.*102T=
XM_011511750.3:c.*37T= XP_011510052.1:n.*37T=
XM_011511756.2:c.917T= XP_011510058.1:p.Leu306=
XM_024453102.1:c.1262T= XP_024308870.1:p.Leu421=
XR_001738918.2:n.1744T=
XR_001738919.2:n.1678T=
XR_923004.3:n.2001T=
XR_923007.3:n.1711T=
XR_923011.3:n.1812T=
NM_152783.5:c.1370T= MANE Select NP_689996.4:p.Leu457=
NM_001287249.2:c.968T= NP_001274178.1:p.Leu323=
NM_001352824.2:c.809T= NP_001339753.1:p.Leu270=
NR_109778.2:n.1241T=