Canonical Allele Identifier: CA1139667389
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 870610
ClinVar RCV Id: RCV001090186
dbSNP Id: rs2068315570

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369878del , CM000685.2:g.38369878del GRCh38
NC_000023.10:g.38229131del , CM000685.1:g.38229131del GRCh37
NC_000023.9:g.38114075del NCBI36
NG_008471.1:g.22396del

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.298+1del
ENST00000643344.1:c.298+1del
ENST00000039007.4:c.298+1del
ENST00000465127.1:c.172-296243del ENSP00000417050.1:n.172-296243del
ENST00000488812.1:n.353+38del
NM_000531.5:c.298+1del
XM_017029556.1:c.298+1del
NM_000531.6:c.298+1del