Canonical Allele Identifier: CA2424882697

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403639G= , CM000685.2:g.38403639G=	GRCh38
NC_000023.10:g.38262892G= , CM000685.1:g.38262892G=	GRCh37
NC_000023.9:g.38147836G=	NCBI36
NG_008471.1:g.56157G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.562G= MANE Select	ENSP00000039007.4:p.Gly188=
ENST00000643344.1:c.*312G=	ENSP00000496606.1:n.*312G=
ENST00000039007.4:c.562G=	ENSP00000039007.4:p.Gly188=
ENST00000465127.1:c.172-262482G=	ENSP00000417050.1:n.172-262482G=
ENST00000488812.1:n.599G=
NM_000531.5:c.562G=	NP_000522.3:p.Gly188=
XM_017029556.1:c.562G=	XP_016885045.1:p.Gly188=
NM_000531.6:c.562G= MANE Select	NP_000522.3:p.Gly188=