Canonical Allele Identifier: CA2231538030
Community Standard Title: NM_001361.5(DHODH):c.595C= (p.Arg199=)
Gene: DHODH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72021201C= , CM000678.2:g.72021201C= GRCh38
NC_000016.9:g.72055100C= , CM000678.1:g.72055100C= GRCh37
NC_000016.8:g.70612601C= NCBI36
NG_016271.1:g.17458C=

Transcript Alleles

HGVS Amino-acid Change
NM_001361.5:c.595C= MANE Select NP_001352.2:p.Arg199=
ENST00000219240.9:c.595C= MANE Select ENSP00000219240.4:p.Arg199=
NM_001361.4:c.595C= NP_001352.2:p.Arg199=
ENST00000219240.8:c.595C= ENSP00000219240.4:p.Arg199=
ENST00000571392.1:n.1485-1964C=
ENST00000572003.5:n.512C=
ENST00000572887.5:c.595C= ENSP00000461848.1:p.Arg199=
ENST00000573922.5:n.314-1964C=
ENST00000574309.5:c.514-2944C=
XM_005255827.2:c.511C= XP_005255884.1:p.Arg171=
XM_005255827.4:c.511C= XP_005255884.1:p.Arg171=
XM_005255828.3:c.187C= XP_005255885.1:p.Arg63=
XM_005255829.2:c.166C= XP_005255886.1:p.Arg56=
XM_005255829.4:c.166C= XP_005255886.1:p.Arg56=
XM_017022990.2:c.268C= XP_016878479.1:p.Arg90=