Canonical Allele Identifier: CA1339784369
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767841T= , CM000664.2:g.241767841T= GRCh38
NC_000002.11:g.242707256T= , CM000664.1:g.242707256T= GRCh37
NC_000002.10:g.242355929T= NCBI36
NG_012012.1:g.38227T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.1438T= MANE Select ENSP00000315351.4:p.Phe480=
ENST00000321264.8:c.1438T= ENSP00000315351.4:p.Phe480=
ENST00000400769.6:c.*188T= ENSP00000383580.2:n.*188T=
ENST00000403782.5:c.1036T= ENSP00000384723.1:p.Phe346=
ENST00000436747.5:c.*2674T= ENSP00000400212.1:n.*2674T=
ENST00000445308.1:c.834T=
ENST00000468064.5:n.1328T=
ENST00000470343.5:n.919T=
ENST00000473126.1:n.637T=
ENST00000486953.5:n.1262T=
ENST00000610344.1:c.*282T= ENSP00000481906.1:n.*282T=
NM_001287249.1:c.1036T= NP_001274178.1:p.Phe346=
NM_152783.4:c.1438T= NP_689996.4:p.Phe480=
NR_109778.1:n.1360T=
XM_011511734.1:c.1558T= XP_011510036.1:p.Phe520=
XM_011511735.1:c.1516T= XP_011510037.1:p.Phe506=
XM_011511736.1:c.1480T= XP_011510038.1:p.Phe494=
XM_011511754.1:c.997T= XP_011510056.1:p.Phe333=
XM_011511755.1:c.988T= XP_011510057.1:p.Phe330=
XM_011511756.1:c.985T= XP_011510058.1:p.Phe329=
XR_923004.1:n.2070T=
XR_923007.1:n.1780T=
XR_923011.1:n.1881T=
NM_001352824.1:c.877T= NP_001339753.1:p.Phe293=
XM_011511734.2:c.1558T= XP_011510036.1:p.Phe520=
XM_011511735.2:c.1516T= XP_011510037.1:p.Phe506=
XM_011511736.2:c.1480T= XP_011510038.1:p.Phe494=
XM_011511756.2:c.985T= XP_011510058.1:p.Phe329=
XM_024453102.1:c.1330T= XP_024308870.1:p.Phe444=
XR_001738918.2:n.1812T=
XR_001738919.2:n.1746T=
XR_923004.3:n.2069T=
XR_923007.3:n.1779T=
XR_923011.3:n.1880T=
NM_152783.5:c.1438T= MANE Select NP_689996.4:p.Phe480=
NM_001287249.2:c.1036T= NP_001274178.1:p.Phe346=
NM_001352824.2:c.877T= NP_001339753.1:p.Phe293=
NR_109778.2:n.1309T=