Canonical Allele Identifier: CA351408720

Gene: D2HGDH

Linked Data

• MyVariant Identifiers: chr2:g.242690719G>T (hg19) ; chr2:g.241751304G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241751304G>T , CM000664.2:g.241751304G>T	GRCh38
NC_000002.11:g.242690719G>T , CM000664.1:g.242690719G>T	GRCh37
NC_000002.10:g.242339392G>T	NCBI36
NG_012012.1:g.21690G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1056G>T MANE Select	ENSP00000315351.4:p.Glu352Asp
ENST00000321264.8:c.1056G>T	ENSP00000315351.4:p.Glu352Asp
ENST00000400769.6:c.854-4545G>T	ENSP00000383580.2:n.854-4545G>T
ENST00000403782.5:c.654G>T	ENSP00000384723.1:p.Glu218Asp
ENST00000432449.1:c.316G>T
ENST00000436747.5:c.*1372G>T	ENSP00000400212.1:n.*1372G>T
ENST00000454048.1:c.159G>T	ENSP00000404596.1:p.Glu53Asp
ENST00000467427.5:n.389+1010G>T
ENST00000470343.5:n.537G>T
ENST00000473126.1:n.255G>T
ENST00000486953.5:n.163+1010G>T
ENST00000496252.5:n.411G>T
NM_001287249.1:c.654G>T	NP_001274178.1:p.Glu218Asp
NM_152783.4:c.1056G>T	NP_689996.4:p.Glu352Asp
NR_109778.1:n.1063-4545G>T
XM_011511734.1:c.1134G>T	XP_011510036.1:p.Glu378Asp
XM_011511735.1:c.1134G>T	XP_011510037.1:p.Glu378Asp
XM_011511736.1:c.1056G>T	XP_011510038.1:p.Glu352Asp
XM_011511737.1:c.1134G>T	XP_011510039.1:p.Glu378Asp
XM_011511742.1:c.1271G>T	XP_011510044.1:p.Arg424Ile
XM_011511743.1:c.1271G>T	XP_011510045.1:p.Arg424Ile
XM_011511744.1:c.1271G>T	XP_011510046.1:p.Arg424Ile
XM_011511745.1:c.1134G>T	XP_011510047.1:p.Glu378Asp
XM_011511748.1:c.1205G>T	XP_011510050.1:p.Arg402Ile
XM_011511749.1:c.1179+1010G>T	XP_011510051.1:n.1179+1010G>T
XM_011511750.1:c.1134G>T	XP_011510052.1:p.Glu378Asp
XM_011511751.1:c.1212+725G>T	XP_011510053.1:n.1212+725G>T
XM_011511753.1:c.1075+1010G>T	XP_011510055.1:n.1075+1010G>T
XM_011511754.1:c.573G>T	XP_011510056.1:p.Glu191Asp
XM_011511755.1:c.564G>T	XP_011510057.1:p.Glu188Asp
XM_011511756.1:c.853+6427G>T	XP_011510058.1:n.853+6427G>T
XM_011511757.1:c.*72G>T	XP_011510059.1:n.*72G>T
XR_241434.3:n.1395G>T
XR_923003.1:n.1917G>T
XR_923004.1:n.1688G>T
XR_923005.1:n.1431G>T
XR_923006.1:n.1431G>T
XR_923007.1:n.1398G>T
XR_923008.1:n.1294G>T
XR_923009.1:n.1294G>T
XR_923010.1:n.1728G>T
XR_923011.1:n.1499G>T
XR_923012.1:n.1433G>T
XR_923014.1:n.1014-4545G>T
NM_001352824.1:c.495G>T	NP_001339753.1:p.Glu165Asp
XM_011511734.2:c.1134G>T	XP_011510036.1:p.Glu378Asp
XM_011511735.2:c.1134G>T	XP_011510037.1:p.Glu378Asp
XM_011511736.2:c.1056G>T	XP_011510038.1:p.Glu352Asp
XM_011511737.3:c.1134G>T	XP_011510039.1:p.Glu378Asp
XM_011511743.2:c.1271G>T	XP_011510045.1:p.Arg424Ile
XM_011511744.2:c.1271G>T	XP_011510046.1:p.Arg424Ile
XM_011511745.3:c.1134G>T	XP_011510047.1:p.Glu378Asp
XM_011511749.3:c.1179+1010G>T	XP_011510051.1:n.1179+1010G>T
XM_011511750.3:c.1134G>T	XP_011510052.1:p.Glu378Asp
XM_011511751.2:c.1212+725G>T	XP_011510053.1:n.1212+725G>T
XM_011511753.3:c.1075+1010G>T	XP_011510055.1:n.1075+1010G>T
XM_011511756.2:c.853+6427G>T	XP_011510058.1:n.853+6427G>T
XM_011511757.3:c.*72G>T	XP_011510059.1:n.*72G>T
XM_017004828.2:c.1056G>T	XP_016860317.1:p.Glu352Asp
XM_017004829.2:c.1271G>T	XP_016860318.1:p.Arg424Ile
XM_017004830.2:c.1134G>T	XP_016860319.1:p.Glu378Asp
XM_024453102.1:c.906G>T	XP_024308870.1:p.Glu302Asp
XR_001738918.2:n.1430G>T
XR_001738919.2:n.1364G>T
XR_002959334.1:n.1916G>T
XR_002959335.1:n.1560G>T
XR_241434.4:n.1394G>T
XR_923004.3:n.1687G>T
XR_923005.2:n.1430G>T
XR_923007.3:n.1397G>T
XR_923009.2:n.1293G>T
XR_923010.2:n.1727G>T
XR_923011.3:n.1498G>T
XR_923012.2:n.1432G>T
XR_923014.3:n.1013-4545G>T
NM_152783.5:c.1056G>T MANE Select	NP_689996.4:p.Glu352Asp
NM_001287249.2:c.654G>T	NP_001274178.1:p.Glu218Asp
NM_001352824.2:c.495G>T	NP_001339753.1:p.Glu165Asp
NR_109778.2:n.1012-4545G>T