Canonical Allele Identifier: CA2231531357
Community Standard Title: NM_001361.5(DHODH):c.403C= (p.Arg135=)
Gene: DHODH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72014641C= , CM000678.2:g.72014641C= GRCh38
NC_000016.9:g.72048540C= , CM000678.1:g.72048540C= GRCh37
NC_000016.8:g.70606041C= NCBI36
NG_016271.1:g.10898C=

Transcript Alleles

HGVS Amino-acid Change
NM_001361.5:c.403C= MANE Select NP_001352.2:p.Arg135=
ENST00000219240.9:c.403C= MANE Select ENSP00000219240.4:p.Arg135=
NM_001361.4:c.403C= NP_001352.2:p.Arg135=
ENST00000219240.8:c.403C= ENSP00000219240.4:p.Arg135=
ENST00000571288.6:c.577C=
ENST00000572003.5:n.223C=
ENST00000572887.5:c.403C= ENSP00000461848.1:p.Arg135=
ENST00000573843.1:n.191C=
ENST00000573922.5:n.199C=
ENST00000574309.5:c.399C=
ENST00000576145.1:c.319C= ENSP00000464333.1:p.Arg107=
XM_005255827.2:c.319C= XP_005255884.1:p.Arg107=
XM_005255827.4:c.319C= XP_005255884.1:p.Arg107=
XM_005255829.4:c.-202C= XP_005255886.1:n.-202C=
XM_017022990.2:c.76C= XP_016878479.1:p.Arg26=