Canonical Allele Identifier: CA224455
Gene: OTC HGNC NCBI

Linked Data

ClinVar Variation Id: 97107
dbSNP Id: rs74518351

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38367335A>G , CM000685.2:g.38367335A>G GRCh38
NC_000023.10:g.38226588A>G , CM000685.1:g.38226588A>G GRCh37
NC_000023.9:g.38111532A>G NCBI36
NG_008471.1:g.19853A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.122A>G MANE Select ENSP00000039007.4:p.Asp41Gly
ENST00000643344.1:c.122A>G ENSP00000496606.1:p.Asp41Gly
ENST00000039007.4:c.122A>G ENSP00000039007.4:p.Asp41Gly
ENST00000465127.1:c.172-298786A>G ENSP00000417050.1:n.172-298786A>G
ENST00000488812.1:n.214A>G
NM_000531.5:c.122A>G NP_000522.3:p.Asp41Gly
XM_017029556.1:c.122A>G XP_016885045.1:p.Asp41Gly
NM_000531.6:c.122A>G MANE Select NP_000522.3:p.Asp41Gly