Canonical Allele Identifier: CA2424882732

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403698C= , CM000685.2:g.38403698C=	GRCh38
NC_000023.10:g.38262951C= , CM000685.1:g.38262951C=	GRCh37
NC_000023.9:g.38147895C=	NCBI36
NG_008471.1:g.56216C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.621C= MANE Select	ENSP00000039007.4:p.Ser207=
ENST00000643344.1:c.*371C=	ENSP00000496606.1:n.*371C=
ENST00000039007.4:c.621C=	ENSP00000039007.4:p.Ser207=
ENST00000465127.1:c.172-262423C=	ENSP00000417050.1:n.172-262423C=
NM_000531.5:c.621C=	NP_000522.3:p.Ser207=
XM_017029556.1:c.621C=	XP_016885045.1:p.Ser207=
NM_000531.6:c.621C= MANE Select	NP_000522.3:p.Ser207=