Canonical Allele Identifier: CA351408880

Gene: D2HGDH

Linked Data

• MyVariant Identifiers: chr2:g.242690798G>A (hg19) ; chr2:g.241751383G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241751383G>A , CM000664.2:g.241751383G>A	GRCh38
NC_000002.11:g.242690798G>A , CM000664.1:g.242690798G>A	GRCh37
NC_000002.10:g.242339471G>A	NCBI36
NG_012012.1:g.21769G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1135G>A MANE Select	ENSP00000315351.4:p.Val379Ile
ENST00000321264.8:c.1135G>A	ENSP00000315351.4:p.Val379Ile
ENST00000400769.6:c.854-4466G>A	ENSP00000383580.2:n.854-4466G>A
ENST00000403782.5:c.733G>A	ENSP00000384723.1:p.Val245Ile
ENST00000432449.1:c.395G>A
ENST00000436747.5:c.*1451G>A	ENSP00000400212.1:n.*1451G>A
ENST00000467427.5:n.389+1089G>A
ENST00000470343.5:n.616G>A
ENST00000473126.1:n.334G>A
ENST00000486953.5:n.163+1089G>A
ENST00000496252.5:n.490G>A
NM_001287249.1:c.733G>A	NP_001274178.1:p.Val245Ile
NM_152783.4:c.1135G>A	NP_689996.4:p.Val379Ile
NR_109778.1:n.1063-4466G>A
XM_011511734.1:c.1213G>A	XP_011510036.1:p.Val405Ile
XM_011511735.1:c.1213G>A	XP_011510037.1:p.Val405Ile
XM_011511736.1:c.1135G>A	XP_011510038.1:p.Val379Ile
XM_011511737.1:c.1213G>A	XP_011510039.1:p.Val405Ile
XM_011511742.1:c.*33G>A	XP_011510044.1:n.*33G>A
XM_011511743.1:c.*33G>A	XP_011510045.1:n.*33G>A
XM_011511744.1:c.*33G>A	XP_011510046.1:n.*33G>A
XM_011511745.1:c.1213G>A	XP_011510047.1:p.Val405Ile
XM_011511748.1:c.*33G>A	XP_011510050.1:n.*33G>A
XM_011511749.1:c.1179+1089G>A	XP_011510051.1:n.1179+1089G>A
XM_011511750.1:c.1213G>A	XP_011510052.1:p.Val405Ile
XM_011511751.1:c.1212+804G>A	XP_011510053.1:n.1212+804G>A
XM_011511753.1:c.1075+1089G>A	XP_011510055.1:n.1075+1089G>A
XM_011511754.1:c.652G>A	XP_011510056.1:p.Val218Ile
XM_011511755.1:c.643G>A	XP_011510057.1:p.Val215Ile
XM_011511756.1:c.853+6506G>A	XP_011510058.1:n.853+6506G>A
XR_241434.3:n.1474G>A
XR_923003.1:n.1996G>A
XR_923004.1:n.1767G>A
XR_923005.1:n.1510G>A
XR_923006.1:n.1510G>A
XR_923007.1:n.1477G>A
XR_923008.1:n.1373G>A
XR_923009.1:n.1373G>A
XR_923010.1:n.1807G>A
XR_923011.1:n.1578G>A
XR_923012.1:n.1512G>A
XR_923014.1:n.1014-4466G>A
NM_001352824.1:c.574G>A	NP_001339753.1:p.Val192Ile
XM_011511734.2:c.1213G>A	XP_011510036.1:p.Val405Ile
XM_011511735.2:c.1213G>A	XP_011510037.1:p.Val405Ile
XM_011511736.2:c.1135G>A	XP_011510038.1:p.Val379Ile
XM_011511737.3:c.1213G>A	XP_011510039.1:p.Val405Ile
XM_011511743.2:c.*33G>A	XP_011510045.1:n.*33G>A
XM_011511744.2:c.*33G>A	XP_011510046.1:n.*33G>A
XM_011511745.3:c.1213G>A	XP_011510047.1:p.Val405Ile
XM_011511749.3:c.1179+1089G>A	XP_011510051.1:n.1179+1089G>A
XM_011511750.3:c.1213G>A	XP_011510052.1:p.Val405Ile
XM_011511751.2:c.1212+804G>A	XP_011510053.1:n.1212+804G>A
XM_011511753.3:c.1075+1089G>A	XP_011510055.1:n.1075+1089G>A
XM_011511756.2:c.853+6506G>A	XP_011510058.1:n.853+6506G>A
XM_017004828.2:c.1135G>A	XP_016860317.1:p.Val379Ile
XM_017004829.2:c.*33G>A	XP_016860318.1:n.*33G>A
XM_017004830.2:c.1213G>A	XP_016860319.1:p.Val405Ile
XM_024453102.1:c.985G>A	XP_024308870.1:p.Val329Ile
XR_001738918.2:n.1509G>A
XR_001738919.2:n.1443G>A
XR_002959334.1:n.1995G>A
XR_002959335.1:n.1639G>A
XR_241434.4:n.1473G>A
XR_923004.3:n.1766G>A
XR_923005.2:n.1509G>A
XR_923007.3:n.1476G>A
XR_923009.2:n.1372G>A
XR_923010.2:n.1806G>A
XR_923011.3:n.1577G>A
XR_923012.2:n.1511G>A
XR_923014.3:n.1013-4466G>A
NM_152783.5:c.1135G>A MANE Select	NP_689996.4:p.Val379Ile
NM_001287249.2:c.733G>A	NP_001274178.1:p.Val245Ile
NM_001352824.2:c.574G>A	NP_001339753.1:p.Val192Ile
NR_109778.2:n.1012-4466G>A