Canonical Allele Identifier: CA2424871665

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38369821C= , CM000685.2:g.38369821C=	GRCh38
NC_000023.10:g.38229074C= , CM000685.1:g.38229074C=	GRCh37
NC_000023.9:g.38114018C=	NCBI36
NG_008471.1:g.22339C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.242C= MANE Select	ENSP00000039007.4:p.Ser81=
ENST00000643344.1:c.242C=	ENSP00000496606.1:p.Ser81=
ENST00000039007.4:c.242C=	ENSP00000039007.4:p.Ser81=
ENST00000465127.1:c.172-296300C=	ENSP00000417050.1:n.172-296300C=
ENST00000488812.1:n.334C=
NM_000531.5:c.242C=	NP_000522.3:p.Ser81=
XM_017029556.1:c.242C=	XP_016885045.1:p.Ser81=
NM_000531.6:c.242C= MANE Select	NP_000522.3:p.Ser81=