Canonical Allele Identifier: CA2231540435
Community Standard Title: NM_001361.5(DHODH):c.1036C= (p.Arg346=)
Gene: DHODH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72023536C= , CM000678.2:g.72023536C= GRCh38
NC_000016.9:g.72057435C= , CM000678.1:g.72057435C= GRCh37
NC_000016.8:g.70614936C= NCBI36
NG_016271.1:g.19793C=

Transcript Alleles

HGVS Amino-acid Change
NM_001361.5:c.1036C= MANE Select NP_001352.2:p.Arg346=
ENST00000219240.9:c.1036C= MANE Select ENSP00000219240.4:p.Arg346=
NM_001361.4:c.1036C= NP_001352.2:p.Arg346=
ENST00000219240.8:c.1036C= ENSP00000219240.4:p.Arg346=
ENST00000571392.1:n.1700C=
ENST00000572887.5:c.1030C= ENSP00000461848.1:p.Arg344=
ENST00000574309.5:c.514-609C=
XM_005255827.2:c.952C= XP_005255884.1:p.Arg318=
XM_005255827.4:c.952C= XP_005255884.1:p.Arg318=
XM_005255828.3:c.628C= XP_005255885.1:p.Arg210=
XM_005255829.2:c.607C= XP_005255886.1:p.Arg203=
XM_005255829.4:c.607C= XP_005255886.1:p.Arg203=
XM_017022990.2:c.709C= XP_016878479.1:p.Arg237=