Canonical Allele Identifier: CA2424885250
Gene: OTC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38411962T= , CM000685.2:g.38411962T= GRCh38
NC_000023.10:g.38271215T= , CM000685.1:g.38271215T= GRCh37
NC_000023.9:g.38156159T= NCBI36
NG_008471.1:g.64480T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.968T= MANE Select ENSP00000039007.4:p.Val323=
ENST00000643344.1:c.*718T= ENSP00000496606.1:n.*718T=
ENST00000039007.4:c.968T= ENSP00000039007.4:p.Val323=
ENST00000465127.1:c.172-254159T= ENSP00000417050.1:n.172-254159T=
NM_000531.5:c.968T= NP_000522.3:p.Val323=
NM_000531.6:c.968T= MANE Select NP_000522.3:p.Val323=