Canonical Allele Identifier: CA1547390860

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233487C= , CM000667.2:g.55233487C=	GRCh38
NC_000005.9:g.54529315C= , CM000667.1:g.54529315C=	GRCh37
NC_000005.8:g.54565072C=	NCBI36
NG_034201.1:g.5231G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.37G= MANE Select	ENSP00000282572.4:p.Ala13=
ENST00000282572.4:c.37G=	ENSP00000282572.4:p.Ala13=
ENST00000501463.2:c.37G=	ENSP00000422485.1:p.Ala13=
NM_021147.4:c.37G=	NP_066970.3:p.Ala13=
NR_125346.1:n.231G=
NR_125347.1:n.231G=
NM_021147.5:c.37G= MANE Select	NP_066970.3:p.Ala13=
NR_125346.2:n.122G=
NR_125347.2:n.122G=