Canonical Allele Identifier: CA2424884368
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38408959C= , CM000685.2:g.38408959C= GRCh38
NC_000023.10:g.38268212C= , CM000685.1:g.38268212C= GRCh37
NC_000023.9:g.38153156C= NCBI36
NG_008471.1:g.61477C=

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.801C= MANE Select ENSP00000039007.4:p.Ser267=
ENST00000643344.1:c.*551C= ENSP00000496606.1:n.*551C=
ENST00000039007.4:c.801C= ENSP00000039007.4:p.Ser267=
ENST00000465127.1:c.172-257162C= ENSP00000417050.1:n.172-257162C=
NM_000531.5:c.801C= NP_000522.3:p.Ser267=
XM_017029556.1:c.801C= XP_016885045.1:p.Ser267=
NM_000531.6:c.801C= MANE Select NP_000522.3:p.Ser267=