Canonical Allele Identifier: CA1339784301
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767726C= , CM000664.2:g.241767726C= GRCh38
NC_000002.11:g.242707141C= , CM000664.1:g.242707141C= GRCh37
NC_000002.10:g.242355814C= NCBI36
NG_012012.1:g.38112C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.1323C= MANE Select ENSP00000315351.4:p.His441=
ENST00000321264.8:c.1323C= ENSP00000315351.4:p.His441=
ENST00000400769.6:c.*73C= ENSP00000383580.2:n.*73C=
ENST00000403782.5:c.921C= ENSP00000384723.1:p.His307=
ENST00000436747.5:c.*2559C= ENSP00000400212.1:n.*2559C=
ENST00000445308.1:c.719C=
ENST00000468064.5:n.1213C=
ENST00000470343.5:n.804C=
ENST00000473126.1:n.522C=
ENST00000486953.5:n.1147C=
ENST00000610344.1:c.*167C= ENSP00000481906.1:n.*167C=
NM_001287249.1:c.921C= NP_001274178.1:p.His307=
NM_152783.4:c.1323C= NP_689996.4:p.His441=
NR_109778.1:n.1245C=
XM_011511734.1:c.1443C= XP_011510036.1:p.His481=
XM_011511735.1:c.1401C= XP_011510037.1:p.His467=
XM_011511736.1:c.1365C= XP_011510038.1:p.His455=
XM_011511744.1:c.*55C= XP_011510046.1:n.*55C=
XM_011511750.1:c.1235C= XP_011510052.1:p.Thr412=
XM_011511754.1:c.882C= XP_011510056.1:p.His294=
XM_011511755.1:c.873C= XP_011510057.1:p.His291=
XM_011511756.1:c.870C= XP_011510058.1:p.His290=
XR_923004.1:n.1955C=
XR_923007.1:n.1665C=
XR_923011.1:n.1766C=
NM_001352824.1:c.762C= NP_001339753.1:p.His254=
XM_011511734.2:c.1443C= XP_011510036.1:p.His481=
XM_011511735.2:c.1401C= XP_011510037.1:p.His467=
XM_011511736.2:c.1365C= XP_011510038.1:p.His455=
XM_011511744.2:c.*55C= XP_011510046.1:n.*55C=
XM_011511750.3:c.1235C= XP_011510052.1:p.Thr412=
XM_011511756.2:c.870C= XP_011510058.1:p.His290=
XM_024453102.1:c.1215C= XP_024308870.1:p.His405=
XR_001738918.2:n.1697C=
XR_001738919.2:n.1631C=
XR_923004.3:n.1954C=
XR_923007.3:n.1664C=
XR_923011.3:n.1765C=
NM_152783.5:c.1323C= MANE Select NP_689996.4:p.His441=
NM_001287249.2:c.921C= NP_001274178.1:p.His307=
NM_001352824.2:c.762C= NP_001339753.1:p.His254=
NR_109778.2:n.1194C=