Canonical Allele Identifier: CA2424882775

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403801C= , CM000685.2:g.38403801C=	GRCh38
NC_000023.10:g.38263054C= , CM000685.1:g.38263054C=	GRCh37
NC_000023.9:g.38147998C=	NCBI36
NG_008471.1:g.56319C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.663+61C= MANE Select	ENSP00000039007.4:n.663+61C=
ENST00000643344.1:c.*413+61C=	ENSP00000496606.1:n.*413+61C=
ENST00000039007.4:c.663+61C=	ENSP00000039007.4:n.663+61C=
ENST00000465127.1:c.172-262320C=	ENSP00000417050.1:n.172-262320C=
NM_000531.5:c.663+61C=	NP_000522.3:n.663+61C=
XM_017029556.1:c.663+61C=	XP_016885045.1:n.663+61C=
NM_000531.6:c.663+61C= MANE Select	NP_000522.3:n.663+61C=