Canonical Allele Identifier: CA1339784347

Gene: D2HGDH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241767801C= , CM000664.2:g.241767801C=	GRCh38
NC_000002.11:g.242707216C= , CM000664.1:g.242707216C=	GRCh37
NC_000002.10:g.242355889C=	NCBI36
NG_012012.1:g.38187C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321264.9:c.1398C= MANE Select	ENSP00000315351.4:p.Ala466=
ENST00000321264.8:c.1398C=	ENSP00000315351.4:p.Ala466=
ENST00000400769.6:c.*148C=	ENSP00000383580.2:n.*148C=
ENST00000403782.5:c.996C=	ENSP00000384723.1:p.Ala332=
ENST00000436747.5:c.*2634C=	ENSP00000400212.1:n.*2634C=
ENST00000445308.1:c.794C=
ENST00000468064.5:n.1288C=
ENST00000470343.5:n.879C=
ENST00000473126.1:n.597C=
ENST00000486953.5:n.1222C=
ENST00000610344.1:c.*242C=	ENSP00000481906.1:n.*242C=
NM_001287249.1:c.996C=	NP_001274178.1:p.Ala332=
NM_152783.4:c.1398C=	NP_689996.4:p.Ala466=
NR_109778.1:n.1320C=
XM_011511734.1:c.1518C=	XP_011510036.1:p.Ala506=
XM_011511735.1:c.1476C=	XP_011510037.1:p.Ala492=
XM_011511736.1:c.1440C=	XP_011510038.1:p.Ala480=
XM_011511750.1:c.*65C=	XP_011510052.1:n.*65C=
XM_011511754.1:c.957C=	XP_011510056.1:p.Ala319=
XM_011511755.1:c.948C=	XP_011510057.1:p.Ala316=
XM_011511756.1:c.945C=	XP_011510058.1:p.Ala315=
XR_923004.1:n.2030C=
XR_923007.1:n.1740C=
XR_923011.1:n.1841C=
NM_001352824.1:c.837C=	NP_001339753.1:p.Ala279=
XM_011511734.2:c.1518C=	XP_011510036.1:p.Ala506=
XM_011511735.2:c.1476C=	XP_011510037.1:p.Ala492=
XM_011511736.2:c.1440C=	XP_011510038.1:p.Ala480=
XM_011511750.3:c.*65C=	XP_011510052.1:n.*65C=
XM_011511756.2:c.945C=	XP_011510058.1:p.Ala315=
XM_024453102.1:c.1290C=	XP_024308870.1:p.Ala430=
XR_001738918.2:n.1772C=
XR_001738919.2:n.1706C=
XR_923004.3:n.2029C=
XR_923007.3:n.1739C=
XR_923011.3:n.1840C=
NM_152783.5:c.1398C= MANE Select	NP_689996.4:p.Ala466=
NM_001287249.2:c.996C=	NP_001274178.1:p.Ala332=
NM_001352824.2:c.837C=	NP_001339753.1:p.Ala279=
NR_109778.2:n.1269C=