Canonical Allele Identifier: CA2558743066
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367132_38367138del , CM000685.2:g.38367132_38367138del GRCh38
NC_000023.10:g.38226385_38226391del , CM000685.1:g.38226385_38226391del GRCh37
NC_000023.9:g.38111329_38111335del NCBI36
NG_008471.1:g.19650_19656del

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.78-159_78-153del MANE Select ENSP00000039007.4:n.78-159_78-153del
ENST00000643344.1:c.78-159_78-153del ENSP00000496606.1:n.78-159_78-153del
ENST00000039007.4:c.78-159_78-153del ENSP00000039007.4:n.78-159_78-153del
ENST00000465127.1:c.172-298989_172-298983del ENSP00000417050.1:n.172-298989_172-298983...
ENST00000488812.1:n.170-159_170-153del
NM_000531.5:c.78-159_78-153del NP_000522.3:n.78-159_78-153del
XM_017029556.1:c.78-159_78-153del XP_016885045.1:n.78-159_78-153del
NM_000531.6:c.78-159_78-153del MANE Select NP_000522.3:n.78-159_78-153del