Canonical Allele Identifier: CA8158682
Community Standard Title: NM_001361.5(DHODH):c.518-11G>A
Gene: DHODH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72021113G>A , CM000678.2:g.72021113G>A GRCh38
NC_000016.9:g.72055012G>A , CM000678.1:g.72055012G>A GRCh37
NC_000016.8:g.70612513G>A NCBI36
NG_016271.1:g.17370G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001361.5:c.518-11G>A MANE Select NP_001352.2:n.518-11G>A
ENST00000219240.9:c.518-11G>A MANE Select ENSP00000219240.4:n.518-11G>A
NM_001361.4:c.518-11G>A NP_001352.2:n.518-11G>A
ENST00000219240.8:c.518-11G>A ENSP00000219240.4:n.518-11G>A
ENST00000571392.1:n.1485-2052G>A
ENST00000572003.5:n.435-11G>A
ENST00000572887.5:c.518-11G>A ENSP00000461848.1:n.518-11G>A
ENST00000573843.1:n.481-11G>A
ENST00000573922.5:n.314-2052G>A
ENST00000574309.5:c.514-3032G>A
XM_005255827.2:c.434-11G>A XP_005255884.1:n.434-11G>A
XM_005255827.4:c.434-11G>A XP_005255884.1:n.434-11G>A
XM_005255828.3:c.110-11G>A XP_005255885.1:n.110-11G>A
XM_005255829.2:c.89-11G>A XP_005255886.1:n.89-11G>A
XM_005255829.4:c.89-11G>A XP_005255886.1:n.89-11G>A
XM_017022990.2:c.191-11G>A XP_016878479.1:n.191-11G>A