Canonical Allele Identifier: CA2231539136
Community Standard Title: NM_001361.5(DHODH):c.730C= (p.Arg244=)
Gene: DHODH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72022386C= , CM000678.2:g.72022386C= GRCh38
NC_000016.9:g.72056285C= , CM000678.1:g.72056285C= GRCh37
NC_000016.8:g.70613786C= NCBI36
NG_016271.1:g.18643C=

Transcript Alleles

HGVS Amino-acid Change
NM_001361.5:c.730C= MANE Select NP_001352.2:p.Arg244=
ENST00000219240.9:c.730C= MANE Select ENSP00000219240.4:p.Arg244=
NM_001361.4:c.730C= NP_001352.2:p.Arg244=
ENST00000219240.8:c.730C= ENSP00000219240.4:p.Arg244=
ENST00000571392.1:n.1485-779C=
ENST00000572887.5:c.730C= ENSP00000461848.1:p.Arg244=
ENST00000573922.5:n.314-779C=
ENST00000574309.5:c.514-1759C=
XM_005255827.2:c.646C= XP_005255884.1:p.Arg216=
XM_005255827.4:c.646C= XP_005255884.1:p.Arg216=
XM_005255828.3:c.322C= XP_005255885.1:p.Arg108=
XM_005255829.2:c.301C= XP_005255886.1:p.Arg101=
XM_005255829.4:c.301C= XP_005255886.1:p.Arg101=
XM_017022990.2:c.403C= XP_016878479.1:p.Arg135=