Canonical Allele Identifier: CA2424882752

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403736C= , CM000685.2:g.38403736C=	GRCh38
NC_000023.10:g.38262989C= , CM000685.1:g.38262989C=	GRCh37
NC_000023.9:g.38147933C=	NCBI36
NG_008471.1:g.56254C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.659C= MANE Select	ENSP00000039007.4:p.Pro220=
ENST00000643344.1:c.*409C=	ENSP00000496606.1:n.*409C=
ENST00000039007.4:c.659C=	ENSP00000039007.4:p.Pro220=
ENST00000465127.1:c.172-262385C=	ENSP00000417050.1:n.172-262385C=
NM_000531.5:c.659C=	NP_000522.3:p.Pro220=
XM_017029556.1:c.659C=	XP_016885045.1:p.Pro220=
NM_000531.6:c.659C= MANE Select	NP_000522.3:p.Pro220=