Canonical Allele Identifier: CA283638576
Community Standard Title: NM_001361.5(DHODH):c.706-250del
Gene: DHODH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72022112del , CM000678.2:g.72022112del GRCh38
NC_000016.9:g.72056011del , CM000678.1:g.72056011del GRCh37
NC_000016.8:g.70613512del NCBI36
NG_016271.1:g.18369del

Transcript Alleles

HGVS Amino-acid Change
NM_001361.5:c.706-250del MANE Select NP_001352.2:n.706-250del
ENST00000219240.9:c.706-250del MANE Select ENSP00000219240.4:n.706-250del
NM_001361.4:c.706-250del NP_001352.2:n.706-250del
ENST00000219240.8:c.706-250del ENSP00000219240.4:n.706-250del
ENST00000571392.1:n.1485-1053del
ENST00000572887.5:c.706-250del ENSP00000461848.1:n.706-250del
ENST00000573922.5:n.314-1053del
ENST00000574309.5:c.514-2033del
XM_005255827.2:c.622-250del XP_005255884.1:n.622-250del
XM_005255827.4:c.622-250del XP_005255884.1:n.622-250del
XM_005255828.3:c.298-250del XP_005255885.1:n.298-250del
XM_005255829.2:c.277-250del XP_005255886.1:n.277-250del
XM_005255829.4:c.277-250del XP_005255886.1:n.277-250del
XM_017022990.2:c.379-250del XP_016878479.1:n.379-250del