Canonical Allele Identifier: CA68571513

Gene: D2HGDH

Linked Data

• dbSNP Id: rs912526378
• gnomAD v2: 2-242707199-G-A
• gnomAD v3: 2-241767784-G-A
• gnomAD v4: 2-241767784-G-A
• MyVariant Identifiers: chr2:g.242707199G>A (hg19) ; chr2:g.241767784G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241767784G>A , CM000664.2:g.241767784G>A	GRCh38
NC_000002.11:g.242707199G>A , CM000664.1:g.242707199G>A	GRCh37
NC_000002.10:g.242355872G>A	NCBI36
NG_012012.1:g.38170G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000321264.9:c.1381G>A MANE Select	ENSP00000315351.4:p.Val461Met
ENST00000321264.8:c.1381G>A	ENSP00000315351.4:p.Val461Met
ENST00000400769.6:c.*131G>A	ENSP00000383580.2:n.*131G>A
ENST00000403782.5:c.979G>A	ENSP00000384723.1:p.Val327Met
ENST00000436747.5:c.*2617G>A	ENSP00000400212.1:n.*2617G>A
ENST00000445308.1:c.777G>A
ENST00000468064.5:n.1271G>A
ENST00000470343.5:n.862G>A
ENST00000473126.1:n.580G>A
ENST00000486953.5:n.1205G>A
ENST00000610344.1:c.*225G>A	ENSP00000481906.1:n.*225G>A
NM_001287249.1:c.979G>A	NP_001274178.1:p.Val327Met
NM_152783.4:c.1381G>A	NP_689996.4:p.Val461Met
NR_109778.1:n.1303G>A
XM_011511734.1:c.1501G>A	XP_011510036.1:p.Val501Met
XM_011511735.1:c.1459G>A	XP_011510037.1:p.Val487Met
XM_011511736.1:c.1423G>A	XP_011510038.1:p.Val475Met
XM_011511744.1:c.*113G>A	XP_011510046.1:n.*113G>A
XM_011511750.1:c.*48G>A	XP_011510052.1:n.*48G>A
XM_011511754.1:c.940G>A	XP_011510056.1:p.Val314Met
XM_011511755.1:c.931G>A	XP_011510057.1:p.Val311Met
XM_011511756.1:c.928G>A	XP_011510058.1:p.Val310Met
XR_923004.1:n.2013G>A
XR_923007.1:n.1723G>A
XR_923011.1:n.1824G>A
NM_001352824.1:c.820G>A	NP_001339753.1:p.Val274Met
XM_011511734.2:c.1501G>A	XP_011510036.1:p.Val501Met
XM_011511735.2:c.1459G>A	XP_011510037.1:p.Val487Met
XM_011511736.2:c.1423G>A	XP_011510038.1:p.Val475Met
XM_011511744.2:c.*113G>A	XP_011510046.1:n.*113G>A
XM_011511750.3:c.*48G>A	XP_011510052.1:n.*48G>A
XM_011511756.2:c.928G>A	XP_011510058.1:p.Val310Met
XM_024453102.1:c.1273G>A	XP_024308870.1:p.Val425Met
XR_001738918.2:n.1755G>A
XR_001738919.2:n.1689G>A
XR_923004.3:n.2012G>A
XR_923007.3:n.1722G>A
XR_923011.3:n.1823G>A
NM_152783.5:c.1381G>A MANE Select	NP_689996.4:p.Val461Met
NM_001287249.2:c.979G>A	NP_001274178.1:p.Val327Met
NM_001352824.2:c.820G>A	NP_001339753.1:p.Val274Met
NR_109778.2:n.1252G>A