Canonical Allele Identifier: CA2424882776

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403803C= , CM000685.2:g.38403803C=	GRCh38
NC_000023.10:g.38263056C= , CM000685.1:g.38263056C=	GRCh37
NC_000023.9:g.38148000C=	NCBI36
NG_008471.1:g.56321C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.663+63C= MANE Select	ENSP00000039007.4:n.663+63C=
ENST00000643344.1:c.*413+63C=	ENSP00000496606.1:n.*413+63C=
ENST00000039007.4:c.663+63C=	ENSP00000039007.4:n.663+63C=
ENST00000465127.1:c.172-262318C=	ENSP00000417050.1:n.172-262318C=
NM_000531.5:c.663+63C=	NP_000522.3:n.663+63C=
XM_017029556.1:c.663+63C=	XP_016885045.1:n.663+63C=
NM_000531.6:c.663+63C= MANE Select	NP_000522.3:n.663+63C=