Canonical Allele Identifier: CA2424885248
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38411956C= , CM000685.2:g.38411956C= GRCh38
NC_000023.10:g.38271209C= , CM000685.1:g.38271209C= GRCh37
NC_000023.9:g.38156153C= NCBI36
NG_008471.1:g.64474C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.962C= MANE Select ENSP00000039007.4:p.Ser321=
ENST00000643344.1:c.*712C= ENSP00000496606.1:n.*712C=
ENST00000039007.4:c.962C= ENSP00000039007.4:p.Ser321=
ENST00000465127.1:c.172-254165C= ENSP00000417050.1:n.172-254165C=
NM_000531.5:c.962C= NP_000522.3:p.Ser321=
NM_000531.6:c.962C= MANE Select NP_000522.3:p.Ser321=