Canonical Allele Identifier: CA1339784333
Gene: D2HGDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241767783C= , CM000664.2:g.241767783C= GRCh38
NC_000002.11:g.242707198C= , CM000664.1:g.242707198C= GRCh37
NC_000002.10:g.242355871C= NCBI36
NG_012012.1:g.38169C=

Transcript Alleles

HGVS Amino-acid change
ENST00000321264.9:c.1380C= MANE Select ENSP00000315351.4:p.His460=
ENST00000321264.8:c.1380C= ENSP00000315351.4:p.His460=
ENST00000400769.6:c.*130C= ENSP00000383580.2:n.*130C=
ENST00000403782.5:c.978C= ENSP00000384723.1:p.His326=
ENST00000436747.5:c.*2616C= ENSP00000400212.1:n.*2616C=
ENST00000445308.1:c.776C=
ENST00000468064.5:n.1270C=
ENST00000470343.5:n.861C=
ENST00000473126.1:n.579C=
ENST00000486953.5:n.1204C=
ENST00000610344.1:c.*224C= ENSP00000481906.1:n.*224C=
NM_001287249.1:c.978C= NP_001274178.1:p.His326=
NM_152783.4:c.1380C= NP_689996.4:p.His460=
NR_109778.1:n.1302C=
XM_011511734.1:c.1500C= XP_011510036.1:p.His500=
XM_011511735.1:c.1458C= XP_011510037.1:p.His486=
XM_011511736.1:c.1422C= XP_011510038.1:p.His474=
XM_011511744.1:c.*112C= XP_011510046.1:n.*112C=
XM_011511750.1:c.*47C= XP_011510052.1:n.*47C=
XM_011511754.1:c.939C= XP_011510056.1:p.His313=
XM_011511755.1:c.930C= XP_011510057.1:p.His310=
XM_011511756.1:c.927C= XP_011510058.1:p.His309=
XR_923004.1:n.2012C=
XR_923007.1:n.1722C=
XR_923011.1:n.1823C=
NM_001352824.1:c.819C= NP_001339753.1:p.His273=
XM_011511734.2:c.1500C= XP_011510036.1:p.His500=
XM_011511735.2:c.1458C= XP_011510037.1:p.His486=
XM_011511736.2:c.1422C= XP_011510038.1:p.His474=
XM_011511744.2:c.*112C= XP_011510046.1:n.*112C=
XM_011511750.3:c.*47C= XP_011510052.1:n.*47C=
XM_011511756.2:c.927C= XP_011510058.1:p.His309=
XM_024453102.1:c.1272C= XP_024308870.1:p.His424=
XR_001738918.2:n.1754C=
XR_001738919.2:n.1688C=
XR_923004.3:n.2011C=
XR_923007.3:n.1721C=
XR_923011.3:n.1822C=
NM_152783.5:c.1380C= MANE Select NP_689996.4:p.His460=
NM_001287249.2:c.978C= NP_001274178.1:p.His326=
NM_001352824.2:c.819C= NP_001339753.1:p.His273=
NR_109778.2:n.1251C=