Canonical Allele Identifier: CA2424866372

Gene: OTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38352693G= , CM000685.2:g.38352693G=	GRCh38
NC_000023.10:g.38211946G= , CM000685.1:g.38211946G=	GRCh37
NC_000023.9:g.38096890G=	NCBI36
NG_008471.1:g.5211G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000039007.5:c.-4G= MANE Select	ENSP00000039007.4:n.-4G=
ENST00000643344.1:c.-4G=	ENSP00000496606.1:n.-4G=
ENST00000039007.4:c.-4G=	ENSP00000039007.4:n.-4G=
ENST00000465127.1:c.172-313428G=	ENSP00000417050.1:n.172-313428G=
ENST00000488812.1:n.89G=
NM_000531.5:c.-4G=	NP_000522.3:n.-4G=
XM_017029556.1:c.-4G=	XP_016885045.1:n.-4G=
NM_000531.6:c.-4G= MANE Select	NP_000522.3:n.-4G=