Canonical Allele Identifier: CA2424881899

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38401434T= , CM000685.2:g.38401434T=	GRCh38
NC_000023.10:g.38260687T= , CM000685.1:g.38260687T=	GRCh37
NC_000023.9:g.38145631T=	NCBI36
NG_008471.1:g.53952T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.540+6T= MANE Select	ENSP00000039007.4:n.540+6T=
ENST00000643344.1:c.*290+6T=	ENSP00000496606.1:n.*290+6T=
ENST00000039007.4:c.540+6T=	ENSP00000039007.4:n.540+6T=
ENST00000465127.1:c.172-264687T=	ENSP00000417050.1:n.172-264687T=
ENST00000488812.1:n.577+6T=
NM_000531.5:c.540+6T=	NP_000522.3:n.540+6T=
XM_017029556.1:c.540+6T=	XP_016885045.1:n.540+6T=
NM_000531.6:c.540+6T= MANE Select	NP_000522.3:n.540+6T=