Canonical Allele Identifier: CA2424871682

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38369851C= , CM000685.2:g.38369851C=	GRCh38
NC_000023.10:g.38229104C= , CM000685.1:g.38229104C=	GRCh37
NC_000023.9:g.38114048C=	NCBI36
NG_008471.1:g.22369C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.272C= MANE Select	ENSP00000039007.4:p.Thr91=
ENST00000643344.1:c.272C=	ENSP00000496606.1:p.Thr91=
ENST00000039007.4:c.272C=	ENSP00000039007.4:p.Thr91=
ENST00000465127.1:c.172-296270C=	ENSP00000417050.1:n.172-296270C=
ENST00000488812.1:n.353+11C=
NM_000531.5:c.272C=	NP_000522.3:p.Thr91=
XM_017029556.1:c.272C=	XP_016885045.1:p.Thr91=
NM_000531.6:c.272C= MANE Select	NP_000522.3:p.Thr91=