Canonical Allele Identifier: CA1339776264
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241751319C= , CM000664.2:g.241751319C= GRCh38
NC_000002.11:g.242690734C= , CM000664.1:g.242690734C= GRCh37
NC_000002.10:g.242339407C= NCBI36
NG_012012.1:g.21705C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.1071C= MANE Select ENSP00000315351.4:p.Phe357=
ENST00000321264.8:c.1071C= ENSP00000315351.4:p.Phe357=
ENST00000400769.6:c.854-4530C= ENSP00000383580.2:n.854-4530C=
ENST00000403782.5:c.669C= ENSP00000384723.1:p.Phe223=
ENST00000432449.1:c.331C=
ENST00000436747.5:c.*1387C= ENSP00000400212.1:n.*1387C=
ENST00000454048.1:c.174C= ENSP00000404596.1:p.Phe58=
ENST00000467427.5:n.389+1025C=
ENST00000470343.5:n.552C=
ENST00000473126.1:n.270C=
ENST00000486953.5:n.163+1025C=
ENST00000496252.5:n.426C=
NM_001287249.1:c.669C= NP_001274178.1:p.Phe223=
NM_152783.4:c.1071C= NP_689996.4:p.Phe357=
NR_109778.1:n.1063-4530C=
XM_011511734.1:c.1149C= XP_011510036.1:p.Phe383=
XM_011511735.1:c.1149C= XP_011510037.1:p.Phe383=
XM_011511736.1:c.1071C= XP_011510038.1:p.Phe357=
XM_011511737.1:c.1149C= XP_011510039.1:p.Phe383=
XM_011511742.1:c.1286C= XP_011510044.1:p.Ser429=
XM_011511743.1:c.1286C= XP_011510045.1:p.Ser429=
XM_011511744.1:c.1286C= XP_011510046.1:p.Ser429=
XM_011511745.1:c.1149C= XP_011510047.1:p.Phe383=
XM_011511748.1:c.1220C= XP_011510050.1:p.Ser407=
XM_011511749.1:c.1179+1025C= XP_011510051.1:n.1179+1025C=
XM_011511750.1:c.1149C= XP_011510052.1:p.Phe383=
XM_011511751.1:c.1212+740C= XP_011510053.1:n.1212+740C=
XM_011511753.1:c.1075+1025C= XP_011510055.1:n.1075+1025C=
XM_011511754.1:c.588C= XP_011510056.1:p.Phe196=
XM_011511755.1:c.579C= XP_011510057.1:p.Phe193=
XM_011511756.1:c.853+6442C= XP_011510058.1:n.853+6442C=
XM_011511757.1:c.*87C= XP_011510059.1:n.*87C=
XR_241434.3:n.1410C=
XR_923003.1:n.1932C=
XR_923004.1:n.1703C=
XR_923005.1:n.1446C=
XR_923006.1:n.1446C=
XR_923007.1:n.1413C=
XR_923008.1:n.1309C=
XR_923009.1:n.1309C=
XR_923010.1:n.1743C=
XR_923011.1:n.1514C=
XR_923012.1:n.1448C=
XR_923014.1:n.1014-4530C=
NM_001352824.1:c.510C= NP_001339753.1:p.Phe170=
XM_011511734.2:c.1149C= XP_011510036.1:p.Phe383=
XM_011511735.2:c.1149C= XP_011510037.1:p.Phe383=
XM_011511736.2:c.1071C= XP_011510038.1:p.Phe357=
XM_011511737.3:c.1149C= XP_011510039.1:p.Phe383=
XM_011511743.2:c.1286C= XP_011510045.1:p.Ser429=
XM_011511744.2:c.1286C= XP_011510046.1:p.Ser429=
XM_011511745.3:c.1149C= XP_011510047.1:p.Phe383=
XM_011511749.3:c.1179+1025C= XP_011510051.1:n.1179+1025C=
XM_011511750.3:c.1149C= XP_011510052.1:p.Phe383=
XM_011511751.2:c.1212+740C= XP_011510053.1:n.1212+740C=
XM_011511753.3:c.1075+1025C= XP_011510055.1:n.1075+1025C=
XM_011511756.2:c.853+6442C= XP_011510058.1:n.853+6442C=
XM_017004828.2:c.1071C= XP_016860317.1:p.Phe357=
XM_017004829.2:c.1286C= XP_016860318.1:p.Ser429=
XM_017004830.2:c.1149C= XP_016860319.1:p.Phe383=
XM_024453102.1:c.921C= XP_024308870.1:p.Phe307=
XR_001738918.2:n.1445C=
XR_001738919.2:n.1379C=
XR_002959334.1:n.1931C=
XR_002959335.1:n.1575C=
XR_241434.4:n.1409C=
XR_923004.3:n.1702C=
XR_923005.2:n.1445C=
XR_923007.3:n.1412C=
XR_923009.2:n.1308C=
XR_923010.2:n.1742C=
XR_923011.3:n.1513C=
XR_923012.2:n.1447C=
XR_923014.3:n.1013-4530C=
NM_152783.5:c.1071C= MANE Select NP_689996.4:p.Phe357=
NM_001287249.2:c.669C= NP_001274178.1:p.Phe223=
NM_001352824.2:c.510C= NP_001339753.1:p.Phe170=
NR_109778.2:n.1012-4530C=