Canonical Allele Identifier: CA1339784362

Gene: D2HGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241767825G= , CM000664.2:g.241767825G=	GRCh38
NC_000002.11:g.242707240G= , CM000664.1:g.242707240G=	GRCh37
NC_000002.10:g.242355913G=	NCBI36
NG_012012.1:g.38211G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1422G= MANE Select	ENSP00000315351.4:p.Ala474=
ENST00000321264.8:c.1422G=	ENSP00000315351.4:p.Ala474=
ENST00000400769.6:c.*172G=	ENSP00000383580.2:n.*172G=
ENST00000403782.5:c.1020G=	ENSP00000384723.1:p.Ala340=
ENST00000436747.5:c.*2658G=	ENSP00000400212.1:n.*2658G=
ENST00000445308.1:c.818G=
ENST00000468064.5:n.1312G=
ENST00000470343.5:n.903G=
ENST00000473126.1:n.621G=
ENST00000486953.5:n.1246G=
ENST00000610344.1:c.*266G=	ENSP00000481906.1:n.*266G=
NM_001287249.1:c.1020G=	NP_001274178.1:p.Ala340=
NM_152783.4:c.1422G=	NP_689996.4:p.Ala474=
NR_109778.1:n.1344G=
XM_011511734.1:c.1542G=	XP_011510036.1:p.Ala514=
XM_011511735.1:c.1500G=	XP_011510037.1:p.Ala500=
XM_011511736.1:c.1464G=	XP_011510038.1:p.Ala488=
XM_011511750.1:c.*89G=	XP_011510052.1:n.*89G=
XM_011511754.1:c.981G=	XP_011510056.1:p.Ala327=
XM_011511755.1:c.972G=	XP_011510057.1:p.Ala324=
XM_011511756.1:c.969G=	XP_011510058.1:p.Ala323=
XR_923004.1:n.2054G=
XR_923007.1:n.1764G=
XR_923011.1:n.1865G=
NM_001352824.1:c.861G=	NP_001339753.1:p.Ala287=
XM_011511734.2:c.1542G=	XP_011510036.1:p.Ala514=
XM_011511735.2:c.1500G=	XP_011510037.1:p.Ala500=
XM_011511736.2:c.1464G=	XP_011510038.1:p.Ala488=
XM_011511750.3:c.*89G=	XP_011510052.1:n.*89G=
XM_011511756.2:c.969G=	XP_011510058.1:p.Ala323=
XM_024453102.1:c.1314G=	XP_024308870.1:p.Ala438=
XR_001738918.2:n.1796G=
XR_001738919.2:n.1730G=
XR_923004.3:n.2053G=
XR_923007.3:n.1763G=
XR_923011.3:n.1864G=
NM_152783.5:c.1422G= MANE Select	NP_689996.4:p.Ala474=
NM_001287249.2:c.1020G=	NP_001274178.1:p.Ala340=
NM_001352824.2:c.861G=	NP_001339753.1:p.Ala287=
NR_109778.2:n.1293G=