Canonical Allele Identifier: CA412725099
Gene: OTC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38403620A>C , CM000685.2:g.38403620A>C GRCh38
NC_000023.10:g.38262873A>C , CM000685.1:g.38262873A>C GRCh37
NC_000023.9:g.38147817A>C NCBI36
NG_008471.1:g.56138A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.543A>C MANE Select ENSP00000039007.4:p.Glu181Asp
ENST00000643344.1:c.*293A>C ENSP00000496606.1:n.*293A>C
ENST00000039007.4:c.543A>C ENSP00000039007.4:p.Glu181Asp
ENST00000465127.1:c.172-262501A>C ENSP00000417050.1:n.172-262501A>C
ENST00000488812.1:n.580A>C
NM_000531.5:c.543A>C NP_000522.3:p.Glu181Asp
XM_017029556.1:c.543A>C XP_016885045.1:p.Glu181Asp
NM_000531.6:c.543A>C MANE Select NP_000522.3:p.Glu181Asp