Canonical Allele Identifier: CA2424882735

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403703C= , CM000685.2:g.38403703C=	GRCh38
NC_000023.10:g.38262956C= , CM000685.1:g.38262956C=	GRCh37
NC_000023.9:g.38147900C=	NCBI36
NG_008471.1:g.56221C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.626C= MANE Select	ENSP00000039007.4:p.Ala209=
ENST00000643344.1:c.*376C=	ENSP00000496606.1:n.*376C=
ENST00000039007.4:c.626C=	ENSP00000039007.4:p.Ala209=
ENST00000465127.1:c.172-262418C=	ENSP00000417050.1:n.172-262418C=
NM_000531.5:c.626C=	NP_000522.3:p.Ala209=
XM_017029556.1:c.626C=	XP_016885045.1:p.Ala209=
NM_000531.6:c.626C= MANE Select	NP_000522.3:p.Ala209=