Canonical Allele Identifier: CA1339784378
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767855C= , CM000664.2:g.241767855C= GRCh38
NC_000002.11:g.242707270C= , CM000664.1:g.242707270C= GRCh37
NC_000002.10:g.242355943C= NCBI36
NG_012012.1:g.38241C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.1452C= MANE Select ENSP00000315351.4:p.Asp484=
ENST00000321264.8:c.1452C= ENSP00000315351.4:p.Asp484=
ENST00000400769.6:c.*202C= ENSP00000383580.2:n.*202C=
ENST00000403782.5:c.1050C= ENSP00000384723.1:p.Asp350=
ENST00000436747.5:c.*2688C= ENSP00000400212.1:n.*2688C=
ENST00000445308.1:c.848C=
ENST00000468064.5:n.1342C=
ENST00000470343.5:n.933C=
ENST00000473126.1:n.651C=
ENST00000486953.5:n.1276C=
ENST00000610344.1:c.*296C= ENSP00000481906.1:n.*296C=
NM_001287249.1:c.1050C= NP_001274178.1:p.Asp350=
NM_152783.4:c.1452C= NP_689996.4:p.Asp484=
NR_109778.1:n.1374C=
XM_011511734.1:c.1572C= XP_011510036.1:p.Asp524=
XM_011511735.1:c.1530C= XP_011510037.1:p.Asp510=
XM_011511736.1:c.1494C= XP_011510038.1:p.Asp498=
XM_011511754.1:c.1011C= XP_011510056.1:p.Asp337=
XM_011511755.1:c.1002C= XP_011510057.1:p.Asp334=
XM_011511756.1:c.999C= XP_011510058.1:p.Asp333=
XR_923004.1:n.2084C=
XR_923007.1:n.1794C=
XR_923011.1:n.1895C=
NM_001352824.1:c.891C= NP_001339753.1:p.Asp297=
XM_011511734.2:c.1572C= XP_011510036.1:p.Asp524=
XM_011511735.2:c.1530C= XP_011510037.1:p.Asp510=
XM_011511736.2:c.1494C= XP_011510038.1:p.Asp498=
XM_011511756.2:c.999C= XP_011510058.1:p.Asp333=
XM_024453102.1:c.1344C= XP_024308870.1:p.Asp448=
XR_001738918.2:n.1826C=
XR_001738919.2:n.1760C=
XR_923004.3:n.2083C=
XR_923007.3:n.1793C=
XR_923011.3:n.1894C=
NM_152783.5:c.1452C= MANE Select NP_689996.4:p.Asp484=
NM_001287249.2:c.1050C= NP_001274178.1:p.Asp350=
NM_001352824.2:c.891C= NP_001339753.1:p.Asp297=
NR_109778.2:n.1323C=