Canonical Allele Identifier: CA1339784318
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767750C= , CM000664.2:g.241767750C= GRCh38
NC_000002.11:g.242707165C= , CM000664.1:g.242707165C= GRCh37
NC_000002.10:g.242355838C= NCBI36
NG_012012.1:g.38136C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000321264.9:c.1347C= MANE Select ENSP00000315351.4:p.Phe449=
ENST00000321264.8:c.1347C= ENSP00000315351.4:p.Phe449=
ENST00000400769.6:c.*97C= ENSP00000383580.2:n.*97C=
ENST00000403782.5:c.945C= ENSP00000384723.1:p.Phe315=
ENST00000436747.5:c.*2583C= ENSP00000400212.1:n.*2583C=
ENST00000445308.1:c.743C=
ENST00000468064.5:n.1237C=
ENST00000470343.5:n.828C=
ENST00000473126.1:n.546C=
ENST00000486953.5:n.1171C=
ENST00000610344.1:c.*191C= ENSP00000481906.1:n.*191C=
NM_001287249.1:c.945C= NP_001274178.1:p.Phe315=
NM_152783.4:c.1347C= NP_689996.4:p.Phe449=
NR_109778.1:n.1269C=
XM_011511734.1:c.1467C= XP_011510036.1:p.Phe489=
XM_011511735.1:c.1425C= XP_011510037.1:p.Phe475=
XM_011511736.1:c.1389C= XP_011510038.1:p.Phe463=
XM_011511744.1:c.*79C= XP_011510046.1:n.*79C=
XM_011511750.1:c.*14C= XP_011510052.1:n.*14C=
XM_011511754.1:c.906C= XP_011510056.1:p.Phe302=
XM_011511755.1:c.897C= XP_011510057.1:p.Phe299=
XM_011511756.1:c.894C= XP_011510058.1:p.Phe298=
XR_923004.1:n.1979C=
XR_923007.1:n.1689C=
XR_923011.1:n.1790C=
NM_001352824.1:c.786C= NP_001339753.1:p.Phe262=
XM_011511734.2:c.1467C= XP_011510036.1:p.Phe489=
XM_011511735.2:c.1425C= XP_011510037.1:p.Phe475=
XM_011511736.2:c.1389C= XP_011510038.1:p.Phe463=
XM_011511744.2:c.*79C= XP_011510046.1:n.*79C=
XM_011511750.3:c.*14C= XP_011510052.1:n.*14C=
XM_011511756.2:c.894C= XP_011510058.1:p.Phe298=
XM_024453102.1:c.1239C= XP_024308870.1:p.Phe413=
XR_001738918.2:n.1721C=
XR_001738919.2:n.1655C=
XR_923004.3:n.1978C=
XR_923007.3:n.1688C=
XR_923011.3:n.1789C=
NM_152783.5:c.1347C= MANE Select NP_689996.4:p.Phe449=
NM_001287249.2:c.945C= NP_001274178.1:p.Phe315=
NM_001352824.2:c.786C= NP_001339753.1:p.Phe262=
NR_109778.2:n.1218C=