Canonical Allele Identifier: CA351413045

Gene: D2HGDH

Linked Data

• MyVariant Identifiers: chr2:g.242707167G>T (hg19) ; chr2:g.241767752G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241767752G>T , CM000664.2:g.241767752G>T	GRCh38
NC_000002.11:g.242707167G>T , CM000664.1:g.242707167G>T	GRCh37
NC_000002.10:g.242355840G>T	NCBI36
NG_012012.1:g.38138G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1349G>T MANE Select	ENSP00000315351.4:p.Ser450Ile
ENST00000321264.8:c.1349G>T	ENSP00000315351.4:p.Ser450Ile
ENST00000400769.6:c.*99G>T	ENSP00000383580.2:n.*99G>T
ENST00000403782.5:c.947G>T	ENSP00000384723.1:p.Ser316Ile
ENST00000436747.5:c.*2585G>T	ENSP00000400212.1:n.*2585G>T
ENST00000445308.1:c.745G>T
ENST00000468064.5:n.1239G>T
ENST00000470343.5:n.830G>T
ENST00000473126.1:n.548G>T
ENST00000486953.5:n.1173G>T
ENST00000610344.1:c.*193G>T	ENSP00000481906.1:n.*193G>T
NM_001287249.1:c.947G>T	NP_001274178.1:p.Ser316Ile
NM_152783.4:c.1349G>T	NP_689996.4:p.Ser450Ile
NR_109778.1:n.1271G>T
XM_011511734.1:c.1469G>T	XP_011510036.1:p.Ser490Ile
XM_011511735.1:c.1427G>T	XP_011510037.1:p.Ser476Ile
XM_011511736.1:c.1391G>T	XP_011510038.1:p.Ser464Ile
XM_011511744.1:c.*81G>T	XP_011510046.1:n.*81G>T
XM_011511750.1:c.*16G>T	XP_011510052.1:n.*16G>T
XM_011511754.1:c.908G>T	XP_011510056.1:p.Ser303Ile
XM_011511755.1:c.899G>T	XP_011510057.1:p.Ser300Ile
XM_011511756.1:c.896G>T	XP_011510058.1:p.Ser299Ile
XR_923004.1:n.1981G>T
XR_923007.1:n.1691G>T
XR_923011.1:n.1792G>T
NM_001352824.1:c.788G>T	NP_001339753.1:p.Ser263Ile
XM_011511734.2:c.1469G>T	XP_011510036.1:p.Ser490Ile
XM_011511735.2:c.1427G>T	XP_011510037.1:p.Ser476Ile
XM_011511736.2:c.1391G>T	XP_011510038.1:p.Ser464Ile
XM_011511744.2:c.*81G>T	XP_011510046.1:n.*81G>T
XM_011511750.3:c.*16G>T	XP_011510052.1:n.*16G>T
XM_011511756.2:c.896G>T	XP_011510058.1:p.Ser299Ile
XM_024453102.1:c.1241G>T	XP_024308870.1:p.Ser414Ile
XR_001738918.2:n.1723G>T
XR_001738919.2:n.1657G>T
XR_923004.3:n.1980G>T
XR_923007.3:n.1690G>T
XR_923011.3:n.1791G>T
NM_152783.5:c.1349G>T MANE Select	NP_689996.4:p.Ser450Ile
NM_001287249.2:c.947G>T	NP_001274178.1:p.Ser316Ile
NM_001352824.2:c.788G>T	NP_001339753.1:p.Ser263Ile
NR_109778.2:n.1220G>T