Canonical Allele Identifier: CA1339776285

Gene: D2HGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241751372A= , CM000664.2:g.241751372A=	GRCh38
NC_000002.11:g.242690787A= , CM000664.1:g.242690787A=	GRCh37
NC_000002.10:g.242339460A=	NCBI36
NG_012012.1:g.21758A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1124A= MANE Select	ENSP00000315351.4:p.Asp375=
ENST00000321264.8:c.1124A=	ENSP00000315351.4:p.Asp375=
ENST00000400769.6:c.854-4477A=	ENSP00000383580.2:n.854-4477A=
ENST00000403782.5:c.722A=	ENSP00000384723.1:p.Asp241=
ENST00000432449.1:c.384A=
ENST00000436747.5:c.*1440A=	ENSP00000400212.1:n.*1440A=
ENST00000454048.1:c.227A=	ENSP00000404596.1:p.Asp76=
ENST00000467427.5:n.389+1078A=
ENST00000470343.5:n.605A=
ENST00000473126.1:n.323A=
ENST00000486953.5:n.163+1078A=
ENST00000496252.5:n.479A=
NM_001287249.1:c.722A=	NP_001274178.1:p.Asp241=
NM_152783.4:c.1124A=	NP_689996.4:p.Asp375=
NR_109778.1:n.1063-4477A=
XM_011511734.1:c.1202A=	XP_011510036.1:p.Asp401=
XM_011511735.1:c.1202A=	XP_011510037.1:p.Asp401=
XM_011511736.1:c.1124A=	XP_011510038.1:p.Asp375=
XM_011511737.1:c.1202A=	XP_011510039.1:p.Asp401=
XM_011511742.1:c.*22A=	XP_011510044.1:n.*22A=
XM_011511743.1:c.*22A=	XP_011510045.1:n.*22A=
XM_011511744.1:c.*22A=	XP_011510046.1:n.*22A=
XM_011511745.1:c.1202A=	XP_011510047.1:p.Asp401=
XM_011511748.1:c.*22A=	XP_011510050.1:n.*22A=
XM_011511749.1:c.1179+1078A=	XP_011510051.1:n.1179+1078A=
XM_011511750.1:c.1202A=	XP_011510052.1:p.Asp401=
XM_011511751.1:c.1212+793A=	XP_011510053.1:n.1212+793A=
XM_011511753.1:c.1075+1078A=	XP_011510055.1:n.1075+1078A=
XM_011511754.1:c.641A=	XP_011510056.1:p.Asp214=
XM_011511755.1:c.632A=	XP_011510057.1:p.Asp211=
XM_011511756.1:c.853+6495A=	XP_011510058.1:n.853+6495A=
XR_241434.3:n.1463A=
XR_923003.1:n.1985A=
XR_923004.1:n.1756A=
XR_923005.1:n.1499A=
XR_923006.1:n.1499A=
XR_923007.1:n.1466A=
XR_923008.1:n.1362A=
XR_923009.1:n.1362A=
XR_923010.1:n.1796A=
XR_923011.1:n.1567A=
XR_923012.1:n.1501A=
XR_923014.1:n.1014-4477A=
NM_001352824.1:c.563A=	NP_001339753.1:p.Asp188=
XM_011511734.2:c.1202A=	XP_011510036.1:p.Asp401=
XM_011511735.2:c.1202A=	XP_011510037.1:p.Asp401=
XM_011511736.2:c.1124A=	XP_011510038.1:p.Asp375=
XM_011511737.3:c.1202A=	XP_011510039.1:p.Asp401=
XM_011511743.2:c.*22A=	XP_011510045.1:n.*22A=
XM_011511744.2:c.*22A=	XP_011510046.1:n.*22A=
XM_011511745.3:c.1202A=	XP_011510047.1:p.Asp401=
XM_011511749.3:c.1179+1078A=	XP_011510051.1:n.1179+1078A=
XM_011511750.3:c.1202A=	XP_011510052.1:p.Asp401=
XM_011511751.2:c.1212+793A=	XP_011510053.1:n.1212+793A=
XM_011511753.3:c.1075+1078A=	XP_011510055.1:n.1075+1078A=
XM_011511756.2:c.853+6495A=	XP_011510058.1:n.853+6495A=
XM_017004828.2:c.1124A=	XP_016860317.1:p.Asp375=
XM_017004829.2:c.*22A=	XP_016860318.1:n.*22A=
XM_017004830.2:c.1202A=	XP_016860319.1:p.Asp401=
XM_024453102.1:c.974A=	XP_024308870.1:p.Asp325=
XR_001738918.2:n.1498A=
XR_001738919.2:n.1432A=
XR_002959334.1:n.1984A=
XR_002959335.1:n.1628A=
XR_241434.4:n.1462A=
XR_923004.3:n.1755A=
XR_923005.2:n.1498A=
XR_923007.3:n.1465A=
XR_923009.2:n.1361A=
XR_923010.2:n.1795A=
XR_923011.3:n.1566A=
XR_923012.2:n.1500A=
XR_923014.3:n.1013-4477A=
NM_152783.5:c.1124A= MANE Select	NP_689996.4:p.Asp375=
NM_001287249.2:c.722A=	NP_001274178.1:p.Asp241=
NM_001352824.2:c.563A=	NP_001339753.1:p.Asp188=
NR_109778.2:n.1012-4477A=