Canonical Allele Identifier: CA2231527911
Community Standard Title: NM_001361.5(DHODH):c.56G= (p.Gly19=)
Gene: DHODH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72012084G= , CM000678.2:g.72012084G= GRCh38
NC_000016.9:g.72045983G= , CM000678.1:g.72045983G= GRCh37
NC_000016.8:g.70603484G= NCBI36
NG_016271.1:g.8341G=

Transcript Alleles

HGVS Amino-acid Change
NM_001361.5:c.56G= MANE Select NP_001352.2:p.Gly19=
ENST00000219240.9:c.56G= MANE Select ENSP00000219240.4:p.Gly19=
NM_001361.4:c.56G= NP_001352.2:p.Gly19=
ENST00000219240.8:c.56G= ENSP00000219240.4:p.Gly19=
ENST00000571288.6:c.43G=
ENST00000572887.5:c.56G= ENSP00000461848.1:p.Gly19=
ENST00000574309.5:c.52G=
ENST00000576145.1:c.-29G= ENSP00000464333.1:n.-29G=
XM_005255827.2:c.-29G= XP_005255884.1:n.-29G=
XM_005255827.4:c.-29G= XP_005255884.1:n.-29G=
XM_017022990.2:c.-373G= XP_016878479.1:n.-373G=