Canonical Allele Identifier: CA351413066

Gene: D2HGDH

Linked Data

• COSMIC: COSM310456
• MyVariant Identifiers: chr2:g.242707181G>A (hg19) ; chr2:g.241767766G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241767766G>A , CM000664.2:g.241767766G>A	GRCh38
NC_000002.11:g.242707181G>A , CM000664.1:g.242707181G>A	GRCh37
NC_000002.10:g.242355854G>A	NCBI36
NG_012012.1:g.38152G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000321264.9:c.1363G>A MANE Select	ENSP00000315351.4:p.Ala455Thr
ENST00000321264.8:c.1363G>A	ENSP00000315351.4:p.Ala455Thr
ENST00000400769.6:c.*113G>A	ENSP00000383580.2:n.*113G>A
ENST00000403782.5:c.961G>A	ENSP00000384723.1:p.Ala321Thr
ENST00000436747.5:c.*2599G>A	ENSP00000400212.1:n.*2599G>A
ENST00000445308.1:c.759G>A
ENST00000468064.5:n.1253G>A
ENST00000470343.5:n.844G>A
ENST00000473126.1:n.562G>A
ENST00000486953.5:n.1187G>A
ENST00000610344.1:c.*207G>A	ENSP00000481906.1:n.*207G>A
NM_001287249.1:c.961G>A	NP_001274178.1:p.Ala321Thr
NM_152783.4:c.1363G>A	NP_689996.4:p.Ala455Thr
NR_109778.1:n.1285G>A
XM_011511734.1:c.1483G>A	XP_011510036.1:p.Ala495Thr
XM_011511735.1:c.1441G>A	XP_011510037.1:p.Ala481Thr
XM_011511736.1:c.1405G>A	XP_011510038.1:p.Ala469Thr
XM_011511744.1:c.*95G>A	XP_011510046.1:n.*95G>A
XM_011511750.1:c.*30G>A	XP_011510052.1:n.*30G>A
XM_011511754.1:c.922G>A	XP_011510056.1:p.Ala308Thr
XM_011511755.1:c.913G>A	XP_011510057.1:p.Ala305Thr
XM_011511756.1:c.910G>A	XP_011510058.1:p.Ala304Thr
XR_923004.1:n.1995G>A
XR_923007.1:n.1705G>A
XR_923011.1:n.1806G>A
NM_001352824.1:c.802G>A	NP_001339753.1:p.Ala268Thr
XM_011511734.2:c.1483G>A	XP_011510036.1:p.Ala495Thr
XM_011511735.2:c.1441G>A	XP_011510037.1:p.Ala481Thr
XM_011511736.2:c.1405G>A	XP_011510038.1:p.Ala469Thr
XM_011511744.2:c.*95G>A	XP_011510046.1:n.*95G>A
XM_011511750.3:c.*30G>A	XP_011510052.1:n.*30G>A
XM_011511756.2:c.910G>A	XP_011510058.1:p.Ala304Thr
XM_024453102.1:c.1255G>A	XP_024308870.1:p.Ala419Thr
XR_001738918.2:n.1737G>A
XR_001738919.2:n.1671G>A
XR_923004.3:n.1994G>A
XR_923007.3:n.1704G>A
XR_923011.3:n.1805G>A
NM_152783.5:c.1363G>A MANE Select	NP_689996.4:p.Ala455Thr
NM_001287249.2:c.961G>A	NP_001274178.1:p.Ala321Thr
NM_001352824.2:c.802G>A	NP_001339753.1:p.Ala268Thr
NR_109778.2:n.1234G>A