Canonical Allele Identifier: CA2231533832

Gene: DHODH

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72017043G= , CM000678.2:g.72017043G=	GRCh38
NC_000016.9:g.72050942G= , CM000678.1:g.72050942G=	GRCh37
NC_000016.8:g.70608443G=	NCBI36
NG_016271.1:g.13300G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001361.5:c.454G= MANE Select	NP_001352.2:p.Gly152=
ENST00000219240.9:c.454G= MANE Select	ENSP00000219240.4:p.Gly152=
NM_001361.4:c.454G=	NP_001352.2:p.Gly152=
ENST00000219240.8:c.454G=	ENSP00000219240.4:p.Gly152=
ENST00000571288.6:c.803G=
ENST00000571392.1:n.1421G=
ENST00000572003.5:n.274G=
ENST00000572887.5:c.454G=	ENSP00000461848.1:p.Gly152=
ENST00000573843.1:n.417G=
ENST00000573922.5:n.250G=
ENST00000574309.5:c.450G=
ENST00000576145.1:c.370G=	ENSP00000464333.1:p.Gly124=
XM_005255827.2:c.370G=	XP_005255884.1:p.Gly124=
XM_005255827.4:c.370G=	XP_005255884.1:p.Gly124=
XM_005255828.3:c.46G=	XP_005255885.1:p.Gly16=
XM_005255829.2:c.25G=	XP_005255886.1:p.Gly9=
XM_005255829.4:c.25G=	XP_005255886.1:p.Gly9=
XM_017022990.2:c.127G=	XP_016878479.1:p.Gly43=