Canonical Allele Identifier: CA2424882716

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38403670A= , CM000685.2:g.38403670A=	GRCh38
NC_000023.10:g.38262923A= , CM000685.1:g.38262923A=	GRCh37
NC_000023.9:g.38147867A=	NCBI36
NG_008471.1:g.56188A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000039007.5:c.593A= MANE Select	ENSP00000039007.4:p.Asn198=
ENST00000643344.1:c.*343A=	ENSP00000496606.1:n.*343A=
ENST00000039007.4:c.593A=	ENSP00000039007.4:p.Asn198=
ENST00000465127.1:c.172-262451A=	ENSP00000417050.1:n.172-262451A=
NM_000531.5:c.593A=	NP_000522.3:p.Asn198=
XM_017029556.1:c.593A=	XP_016885045.1:p.Asn198=
NM_000531.6:c.593A= MANE Select	NP_000522.3:p.Asn198=