Canonical Allele Identifier: CA1339784302
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767727C= , CM000664.2:g.241767727C= GRCh38
NC_000002.11:g.242707142C= , CM000664.1:g.242707142C= GRCh37
NC_000002.10:g.242355815C= NCBI36
NG_012012.1:g.38113C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.1324C= MANE Select ENSP00000315351.4:p.Leu442=
ENST00000321264.8:c.1324C= ENSP00000315351.4:p.Leu442=
ENST00000400769.6:c.*74C= ENSP00000383580.2:n.*74C=
ENST00000403782.5:c.922C= ENSP00000384723.1:p.Leu308=
ENST00000436747.5:c.*2560C= ENSP00000400212.1:n.*2560C=
ENST00000445308.1:c.720C=
ENST00000468064.5:n.1214C=
ENST00000470343.5:n.805C=
ENST00000473126.1:n.523C=
ENST00000486953.5:n.1148C=
ENST00000610344.1:c.*168C= ENSP00000481906.1:n.*168C=
NM_001287249.1:c.922C= NP_001274178.1:p.Leu308=
NM_152783.4:c.1324C= NP_689996.4:p.Leu442=
NR_109778.1:n.1246C=
XM_011511734.1:c.1444C= XP_011510036.1:p.Leu482=
XM_011511735.1:c.1402C= XP_011510037.1:p.Leu468=
XM_011511736.1:c.1366C= XP_011510038.1:p.Leu456=
XM_011511744.1:c.*56C= XP_011510046.1:n.*56C=
XM_011511750.1:c.1236C= XP_011510052.1:p.Thr412=
XM_011511754.1:c.883C= XP_011510056.1:p.Leu295=
XM_011511755.1:c.874C= XP_011510057.1:p.Leu292=
XM_011511756.1:c.871C= XP_011510058.1:p.Leu291=
XR_923004.1:n.1956C=
XR_923007.1:n.1666C=
XR_923011.1:n.1767C=
NM_001352824.1:c.763C= NP_001339753.1:p.Leu255=
XM_011511734.2:c.1444C= XP_011510036.1:p.Leu482=
XM_011511735.2:c.1402C= XP_011510037.1:p.Leu468=
XM_011511736.2:c.1366C= XP_011510038.1:p.Leu456=
XM_011511744.2:c.*56C= XP_011510046.1:n.*56C=
XM_011511750.3:c.1236C= XP_011510052.1:p.Thr412=
XM_011511756.2:c.871C= XP_011510058.1:p.Leu291=
XM_024453102.1:c.1216C= XP_024308870.1:p.Leu406=
XR_001738918.2:n.1698C=
XR_001738919.2:n.1632C=
XR_923004.3:n.1955C=
XR_923007.3:n.1665C=
XR_923011.3:n.1766C=
NM_152783.5:c.1324C= MANE Select NP_689996.4:p.Leu442=
NM_001287249.2:c.922C= NP_001274178.1:p.Leu308=
NM_001352824.2:c.763C= NP_001339753.1:p.Leu255=
NR_109778.2:n.1195C=