Canonical Allele Identifier: CA2231538060
Community Standard Title: NM_001361.5(DHODH):c.605G= (p.Gly202=)
Gene: DHODH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72021211G= , CM000678.2:g.72021211G= GRCh38
NC_000016.9:g.72055110G= , CM000678.1:g.72055110G= GRCh37
NC_000016.8:g.70612611G= NCBI36
NG_016271.1:g.17468G=

Transcript Alleles

HGVS Amino-acid Change
NM_001361.5:c.605G= MANE Select NP_001352.2:p.Gly202=
ENST00000219240.9:c.605G= MANE Select ENSP00000219240.4:p.Gly202=
NM_001361.4:c.605G= NP_001352.2:p.Gly202=
ENST00000219240.8:c.605G= ENSP00000219240.4:p.Gly202=
ENST00000571392.1:n.1485-1954G=
ENST00000572003.5:n.522G=
ENST00000572887.5:c.605G= ENSP00000461848.1:p.Gly202=
ENST00000573922.5:n.314-1954G=
ENST00000574309.5:c.514-2934G=
XM_005255827.2:c.521G= XP_005255884.1:p.Gly174=
XM_005255827.4:c.521G= XP_005255884.1:p.Gly174=
XM_005255828.3:c.197G= XP_005255885.1:p.Gly66=
XM_005255829.2:c.176G= XP_005255886.1:p.Gly59=
XM_005255829.4:c.176G= XP_005255886.1:p.Gly59=
XM_017022990.2:c.278G= XP_016878479.1:p.Gly93=