Canonical Allele Identifier: CA2424870790
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367294T= , CM000685.2:g.38367294T= GRCh38
NC_000023.10:g.38226547T= , CM000685.1:g.38226547T= GRCh37
NC_000023.9:g.38111491T= NCBI36
NG_008471.1:g.19812T=

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.81T= MANE Select ENSP00000039007.4:p.Cys27=
ENST00000643344.1:c.81T= ENSP00000496606.1:p.Cys27=
ENST00000039007.4:c.81T= ENSP00000039007.4:p.Cys27=
ENST00000465127.1:c.172-298827T= ENSP00000417050.1:n.172-298827T=
ENST00000488812.1:n.173T=
NM_000531.5:c.81T= NP_000522.3:p.Cys27=
XM_017029556.1:c.81T= XP_016885045.1:p.Cys27=
NM_000531.6:c.81T= MANE Select NP_000522.3:p.Cys27=