Canonical Allele Identifier: CA224619
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 10991
dbSNP Id: rs72556267

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38401348G>T , CM000685.2:g.38401348G>T GRCh38
NC_000023.10:g.38260601G>T , CM000685.1:g.38260601G>T GRCh37
NC_000023.9:g.38145545G>T NCBI36
NG_008471.1:g.53866G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.460G>T MANE Select ENSP00000039007.4:p.Glu154Ter
ENST00000643344.1:c.*210G>T ENSP00000496606.1:n.*210G>T
ENST00000039007.4:c.460G>T ENSP00000039007.4:p.Glu154Ter
ENST00000465127.1:c.172-264773G>T ENSP00000417050.1:n.172-264773G>T
ENST00000488812.1:n.497G>T
NM_000531.5:c.460G>T NP_000522.3:p.Glu154Ter
XM_017029556.1:c.460G>T XP_016885045.1:p.Glu154Ter
NM_000531.6:c.460G>T MANE Select NP_000522.3:p.Glu154Ter