Canonical Allele Identifier: CA412726154
Gene: OTC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38411922G>A , CM000685.2:g.38411922G>A GRCh38
NC_000023.10:g.38271175G>A , CM000685.1:g.38271175G>A GRCh37
NC_000023.9:g.38156119G>A NCBI36
NG_008471.1:g.64440G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.928G>A MANE Select ENSP00000039007.4:p.Glu310Lys
ENST00000643344.1:c.*678G>A ENSP00000496606.1:n.*678G>A
ENST00000039007.4:c.928G>A ENSP00000039007.4:p.Glu310Lys
ENST00000465127.1:c.172-254199G>A ENSP00000417050.1:n.172-254199G>A
NM_000531.5:c.928G>A NP_000522.3:p.Glu310Lys
NM_000531.6:c.928G>A MANE Select NP_000522.3:p.Glu310Lys