Canonical Allele Identifier: CA412716813
Gene: OTC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369808T>A , CM000685.2:g.38369808T>A GRCh38
NC_000023.10:g.38229061T>A , CM000685.1:g.38229061T>A GRCh37
NC_000023.9:g.38114005T>A NCBI36
NG_008471.1:g.22326T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.229T>A MANE Select ENSP00000039007.4:p.Leu77Met
ENST00000643344.1:c.229T>A ENSP00000496606.1:p.Leu77Met
ENST00000039007.4:c.229T>A ENSP00000039007.4:p.Leu77Met
ENST00000465127.1:c.172-296313T>A ENSP00000417050.1:n.172-296313T>A
ENST00000488812.1:n.321T>A
NM_000531.5:c.229T>A NP_000522.3:p.Leu77Met
XM_017029556.1:c.229T>A XP_016885045.1:p.Leu77Met
NM_000531.6:c.229T>A MANE Select NP_000522.3:p.Leu77Met