Canonical Allele Identifier: CA312796
Gene: OTC HGNC NCBI

Linked Data

dbSNP Id: rs796052011

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367277A>G , CM000685.2:g.38367277A>G GRCh38
NC_000023.10:g.38226530A>G , CM000685.1:g.38226530A>G GRCh37
NC_000023.9:g.38111474A>G NCBI36
NG_008471.1:g.19795A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.78-14A>G MANE Select ENSP00000039007.4:n.78-14A>G
ENST00000643344.1:c.78-14A>G ENSP00000496606.1:n.78-14A>G
ENST00000039007.4:c.78-14A>G ENSP00000039007.4:n.78-14A>G
ENST00000465127.1:c.172-298844A>G ENSP00000417050.1:n.172-298844A>G
ENST00000488812.1:n.170-14A>G
NM_000531.5:c.78-14A>G NP_000522.3:n.78-14A>G
XM_017029556.1:c.78-14A>G XP_016885045.1:n.78-14A>G
NM_000531.6:c.78-14A>G MANE Select NP_000522.3:n.78-14A>G