Canonical Allele Identifier: CA2424870840

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38367409A= , CM000685.2:g.38367409A=	GRCh38
NC_000023.10:g.38226662A= , CM000685.1:g.38226662A=	GRCh37
NC_000023.9:g.38111606A=	NCBI36
NG_008471.1:g.19927A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.196A= MANE Select	ENSP00000039007.4:p.Arg66=
ENST00000643344.1:c.196A=	ENSP00000496606.1:p.Arg66=
ENST00000039007.4:c.196A=	ENSP00000039007.4:p.Arg66=
ENST00000465127.1:c.172-298712A=	ENSP00000417050.1:n.172-298712A=
ENST00000488812.1:n.288A=
NM_000531.5:c.196A=	NP_000522.3:p.Arg66=
XM_017029556.1:c.196A=	XP_016885045.1:p.Arg66=
NM_000531.6:c.196A= MANE Select	NP_000522.3:p.Arg66=