Canonical Allele Identifier: CA351413285
Gene: D2HGDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767811G>A , CM000664.2:g.241767811G>A GRCh38
NC_000002.11:g.242707226G>A , CM000664.1:g.242707226G>A GRCh37
NC_000002.10:g.242355899G>A NCBI36
NG_012012.1:g.38197G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.1408G>A MANE Select ENSP00000315351.4:p.Gly470Ser
ENST00000321264.8:c.1408G>A ENSP00000315351.4:p.Gly470Ser
ENST00000400769.6:c.*158G>A ENSP00000383580.2:n.*158G>A
ENST00000403782.5:c.1006G>A ENSP00000384723.1:p.Gly336Ser
ENST00000436747.5:c.*2644G>A ENSP00000400212.1:n.*2644G>A
ENST00000445308.1:c.804G>A
ENST00000468064.5:n.1298G>A
ENST00000470343.5:n.889G>A
ENST00000473126.1:n.607G>A
ENST00000486953.5:n.1232G>A
ENST00000610344.1:c.*252G>A ENSP00000481906.1:n.*252G>A
NM_001287249.1:c.1006G>A NP_001274178.1:p.Gly336Ser
NM_152783.4:c.1408G>A NP_689996.4:p.Gly470Ser
NR_109778.1:n.1330G>A
XM_011511734.1:c.1528G>A XP_011510036.1:p.Gly510Ser
XM_011511735.1:c.1486G>A XP_011510037.1:p.Gly496Ser
XM_011511736.1:c.1450G>A XP_011510038.1:p.Gly484Ser
XM_011511750.1:c.*75G>A XP_011510052.1:n.*75G>A
XM_011511754.1:c.967G>A XP_011510056.1:p.Gly323Ser
XM_011511755.1:c.958G>A XP_011510057.1:p.Gly320Ser
XM_011511756.1:c.955G>A XP_011510058.1:p.Gly319Ser
XR_923004.1:n.2040G>A
XR_923007.1:n.1750G>A
XR_923011.1:n.1851G>A
NM_001352824.1:c.847G>A NP_001339753.1:p.Gly283Ser
XM_011511734.2:c.1528G>A XP_011510036.1:p.Gly510Ser
XM_011511735.2:c.1486G>A XP_011510037.1:p.Gly496Ser
XM_011511736.2:c.1450G>A XP_011510038.1:p.Gly484Ser
XM_011511750.3:c.*75G>A XP_011510052.1:n.*75G>A
XM_011511756.2:c.955G>A XP_011510058.1:p.Gly319Ser
XM_024453102.1:c.1300G>A XP_024308870.1:p.Gly434Ser
XR_001738918.2:n.1782G>A
XR_001738919.2:n.1716G>A
XR_923004.3:n.2039G>A
XR_923007.3:n.1749G>A
XR_923011.3:n.1850G>A
NM_152783.5:c.1408G>A MANE Select NP_689996.4:p.Gly470Ser
NM_001287249.2:c.1006G>A NP_001274178.1:p.Gly336Ser
NM_001352824.2:c.847G>A NP_001339753.1:p.Gly283Ser
NR_109778.2:n.1279G>A