Canonical Allele Identifier: CA351413098

Gene: D2HGDH

Linked Data

• MyVariant Identifiers: chr2:g.242707196C>G (hg19) ; chr2:g.241767781C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241767781C>G , CM000664.2:g.241767781C>G	GRCh38
NC_000002.11:g.242707196C>G , CM000664.1:g.242707196C>G	GRCh37
NC_000002.10:g.242355869C>G	NCBI36
NG_012012.1:g.38167C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1378C>G MANE Select	ENSP00000315351.4:p.His460Asp
ENST00000321264.8:c.1378C>G	ENSP00000315351.4:p.His460Asp
ENST00000400769.6:c.*128C>G	ENSP00000383580.2:n.*128C>G
ENST00000403782.5:c.976C>G	ENSP00000384723.1:p.His326Asp
ENST00000436747.5:c.*2614C>G	ENSP00000400212.1:n.*2614C>G
ENST00000445308.1:c.774C>G
ENST00000468064.5:n.1268C>G
ENST00000470343.5:n.859C>G
ENST00000473126.1:n.577C>G
ENST00000486953.5:n.1202C>G
ENST00000610344.1:c.*222C>G	ENSP00000481906.1:n.*222C>G
NM_001287249.1:c.976C>G	NP_001274178.1:p.His326Asp
NM_152783.4:c.1378C>G	NP_689996.4:p.His460Asp
NR_109778.1:n.1300C>G
XM_011511734.1:c.1498C>G	XP_011510036.1:p.His500Asp
XM_011511735.1:c.1456C>G	XP_011510037.1:p.His486Asp
XM_011511736.1:c.1420C>G	XP_011510038.1:p.His474Asp
XM_011511744.1:c.*110C>G	XP_011510046.1:n.*110C>G
XM_011511750.1:c.*45C>G	XP_011510052.1:n.*45C>G
XM_011511754.1:c.937C>G	XP_011510056.1:p.His313Asp
XM_011511755.1:c.928C>G	XP_011510057.1:p.His310Asp
XM_011511756.1:c.925C>G	XP_011510058.1:p.His309Asp
XR_923004.1:n.2010C>G
XR_923007.1:n.1720C>G
XR_923011.1:n.1821C>G
NM_001352824.1:c.817C>G	NP_001339753.1:p.His273Asp
XM_011511734.2:c.1498C>G	XP_011510036.1:p.His500Asp
XM_011511735.2:c.1456C>G	XP_011510037.1:p.His486Asp
XM_011511736.2:c.1420C>G	XP_011510038.1:p.His474Asp
XM_011511744.2:c.*110C>G	XP_011510046.1:n.*110C>G
XM_011511750.3:c.*45C>G	XP_011510052.1:n.*45C>G
XM_011511756.2:c.925C>G	XP_011510058.1:p.His309Asp
XM_024453102.1:c.1270C>G	XP_024308870.1:p.His424Asp
XR_001738918.2:n.1752C>G
XR_001738919.2:n.1686C>G
XR_923004.3:n.2009C>G
XR_923007.3:n.1719C>G
XR_923011.3:n.1820C>G
NM_152783.5:c.1378C>G MANE Select	NP_689996.4:p.His460Asp
NM_001287249.2:c.976C>G	NP_001274178.1:p.His326Asp
NM_001352824.2:c.817C>G	NP_001339753.1:p.His273Asp
NR_109778.2:n.1249C>G