Canonical Allele Identifier: CA1547390607

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233319C= , CM000667.2:g.55233319C=	GRCh38
NC_000005.9:g.54529147C= , CM000667.1:g.54529147C=	GRCh37
NC_000005.8:g.54564904C=	NCBI36
NG_034201.1:g.5399G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.205G= MANE Select	ENSP00000282572.4:p.Asp69=
ENST00000282572.4:c.205G=	ENSP00000282572.4:p.Asp69=
ENST00000501463.2:c.205G=	ENSP00000422485.1:p.Asp69=
NM_021147.4:c.205G=	NP_066970.3:p.Asp69=
NR_125346.1:n.399G=
NR_125347.1:n.399G=
NM_021147.5:c.205G= MANE Select	NP_066970.3:p.Asp69=
NR_125346.2:n.290G=
NR_125347.2:n.290G=