Canonical Allele Identifier: CA1339784349
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767803G= , CM000664.2:g.241767803G= GRCh38
NC_000002.11:g.242707218G= , CM000664.1:g.242707218G= GRCh37
NC_000002.10:g.242355891G= NCBI36
NG_012012.1:g.38189G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.1400G= MANE Select ENSP00000315351.4:p.Gly467=
ENST00000321264.8:c.1400G= ENSP00000315351.4:p.Gly467=
ENST00000400769.6:c.*150G= ENSP00000383580.2:n.*150G=
ENST00000403782.5:c.998G= ENSP00000384723.1:p.Gly333=
ENST00000436747.5:c.*2636G= ENSP00000400212.1:n.*2636G=
ENST00000445308.1:c.796G=
ENST00000468064.5:n.1290G=
ENST00000470343.5:n.881G=
ENST00000473126.1:n.599G=
ENST00000486953.5:n.1224G=
ENST00000610344.1:c.*244G= ENSP00000481906.1:n.*244G=
NM_001287249.1:c.998G= NP_001274178.1:p.Gly333=
NM_152783.4:c.1400G= NP_689996.4:p.Gly467=
NR_109778.1:n.1322G=
XM_011511734.1:c.1520G= XP_011510036.1:p.Gly507=
XM_011511735.1:c.1478G= XP_011510037.1:p.Gly493=
XM_011511736.1:c.1442G= XP_011510038.1:p.Gly481=
XM_011511750.1:c.*67G= XP_011510052.1:n.*67G=
XM_011511754.1:c.959G= XP_011510056.1:p.Gly320=
XM_011511755.1:c.950G= XP_011510057.1:p.Gly317=
XM_011511756.1:c.947G= XP_011510058.1:p.Gly316=
XR_923004.1:n.2032G=
XR_923007.1:n.1742G=
XR_923011.1:n.1843G=
NM_001352824.1:c.839G= NP_001339753.1:p.Gly280=
XM_011511734.2:c.1520G= XP_011510036.1:p.Gly507=
XM_011511735.2:c.1478G= XP_011510037.1:p.Gly493=
XM_011511736.2:c.1442G= XP_011510038.1:p.Gly481=
XM_011511750.3:c.*67G= XP_011510052.1:n.*67G=
XM_011511756.2:c.947G= XP_011510058.1:p.Gly316=
XM_024453102.1:c.1292G= XP_024308870.1:p.Gly431=
XR_001738918.2:n.1774G=
XR_001738919.2:n.1708G=
XR_923004.3:n.2031G=
XR_923007.3:n.1741G=
XR_923011.3:n.1842G=
NM_152783.5:c.1400G= MANE Select NP_689996.4:p.Gly467=
NM_001287249.2:c.998G= NP_001274178.1:p.Gly333=
NM_001352824.2:c.839G= NP_001339753.1:p.Gly280=
NR_109778.2:n.1271G=