Canonical Allele Identifier: CA1339784372
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767845G= , CM000664.2:g.241767845G= GRCh38
NC_000002.11:g.242707260G= , CM000664.1:g.242707260G= GRCh37
NC_000002.10:g.242355933G= NCBI36
NG_012012.1:g.38231G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.1442G= MANE Select ENSP00000315351.4:p.Arg481=
ENST00000321264.8:c.1442G= ENSP00000315351.4:p.Arg481=
ENST00000400769.6:c.*192G= ENSP00000383580.2:n.*192G=
ENST00000403782.5:c.1040G= ENSP00000384723.1:p.Arg347=
ENST00000436747.5:c.*2678G= ENSP00000400212.1:n.*2678G=
ENST00000445308.1:c.838G=
ENST00000468064.5:n.1332G=
ENST00000470343.5:n.923G=
ENST00000473126.1:n.641G=
ENST00000486953.5:n.1266G=
ENST00000610344.1:c.*286G= ENSP00000481906.1:n.*286G=
NM_001287249.1:c.1040G= NP_001274178.1:p.Arg347=
NM_152783.4:c.1442G= NP_689996.4:p.Arg481=
NR_109778.1:n.1364G=
XM_011511734.1:c.1562G= XP_011510036.1:p.Arg521=
XM_011511735.1:c.1520G= XP_011510037.1:p.Arg507=
XM_011511736.1:c.1484G= XP_011510038.1:p.Arg495=
XM_011511754.1:c.1001G= XP_011510056.1:p.Arg334=
XM_011511755.1:c.992G= XP_011510057.1:p.Arg331=
XM_011511756.1:c.989G= XP_011510058.1:p.Arg330=
XR_923004.1:n.2074G=
XR_923007.1:n.1784G=
XR_923011.1:n.1885G=
NM_001352824.1:c.881G= NP_001339753.1:p.Arg294=
XM_011511734.2:c.1562G= XP_011510036.1:p.Arg521=
XM_011511735.2:c.1520G= XP_011510037.1:p.Arg507=
XM_011511736.2:c.1484G= XP_011510038.1:p.Arg495=
XM_011511756.2:c.989G= XP_011510058.1:p.Arg330=
XM_024453102.1:c.1334G= XP_024308870.1:p.Arg445=
XR_001738918.2:n.1816G=
XR_001738919.2:n.1750G=
XR_923004.3:n.2073G=
XR_923007.3:n.1783G=
XR_923011.3:n.1884G=
NM_152783.5:c.1442G= MANE Select NP_689996.4:p.Arg481=
NM_001287249.2:c.1040G= NP_001274178.1:p.Arg347=
NM_001352824.2:c.881G= NP_001339753.1:p.Arg294=
NR_109778.2:n.1313G=