Canonical Allele Identifier: CA1547396713

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233196T= , CM000667.2:g.55233196T=	GRCh38
NC_000005.9:g.54529024T= , CM000667.1:g.54529024T=	GRCh37
NC_000005.8:g.54564781T=	NCBI36
NG_034201.1:g.5522A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.328A= MANE Select	ENSP00000282572.4:p.Lys110=
ENST00000282572.4:c.328A=	ENSP00000282572.4:p.Lys110=
ENST00000501463.2:c.328A=	ENSP00000422485.1:p.Lys110=
NM_021147.4:c.328A=	NP_066970.3:p.Lys110=
NR_125346.1:n.522A=
NR_125347.1:n.522A=
NM_021147.5:c.328A= MANE Select	NP_066970.3:p.Lys110=
NR_125346.2:n.413A=
NR_125347.2:n.413A=