Canonical Allele Identifier: CA224727
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 97281
ClinVar RCV Id: RCV000083525
dbSNP Id: rs72558425

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38403735C>G , CM000685.2:g.38403735C>G GRCh38
NC_000023.10:g.38262988C>G , CM000685.1:g.38262988C>G GRCh37
NC_000023.9:g.38147932C>G NCBI36
NG_008471.1:g.56253C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.658C>G MANE Select ENSP00000039007.4:p.Pro220Ala
ENST00000643344.1:c.*408C>G ENSP00000496606.1:n.*408C>G
ENST00000039007.4:c.658C>G ENSP00000039007.4:p.Pro220Ala
ENST00000465127.1:c.172-262386C>G ENSP00000417050.1:n.172-262386C>G
NM_000531.5:c.658C>G NP_000522.3:p.Pro220Ala
XM_017029556.1:c.658C>G XP_016885045.1:p.Pro220Ala
NM_000531.6:c.658C>G MANE Select NP_000522.3:p.Pro220Ala