Canonical Allele Identifier: CA412723778
Gene: OTC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38401388A>C , CM000685.2:g.38401388A>C GRCh38
NC_000023.10:g.38260641A>C , CM000685.1:g.38260641A>C GRCh37
NC_000023.9:g.38145585A>C NCBI36
NG_008471.1:g.53906A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.500A>C MANE Select ENSP00000039007.4:p.Tyr167Ser
ENST00000643344.1:c.*250A>C ENSP00000496606.1:n.*250A>C
ENST00000039007.4:c.500A>C ENSP00000039007.4:p.Tyr167Ser
ENST00000465127.1:c.172-264733A>C ENSP00000417050.1:n.172-264733A>C
ENST00000488812.1:n.537A>C
NM_000531.5:c.500A>C NP_000522.3:p.Tyr167Ser
XM_017029556.1:c.500A>C XP_016885045.1:p.Tyr167Ser
NM_000531.6:c.500A>C MANE Select NP_000522.3:p.Tyr167Ser