Canonical Allele Identifier: CA1547390773

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233427T= , CM000667.2:g.55233427T=	GRCh38
NC_000005.9:g.54529255T= , CM000667.1:g.54529255T=	GRCh37
NC_000005.8:g.54565012T=	NCBI36
NG_034201.1:g.5291A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.97A= MANE Select	ENSP00000282572.4:p.Arg33=
ENST00000282572.4:c.97A=	ENSP00000282572.4:p.Arg33=
ENST00000501463.2:c.97A=	ENSP00000422485.1:p.Arg33=
NM_021147.4:c.97A=	NP_066970.3:p.Arg33=
NR_125346.1:n.291A=
NR_125347.1:n.291A=
NM_021147.5:c.97A= MANE Select	NP_066970.3:p.Arg33=
NR_125346.2:n.182A=
NR_125347.2:n.182A=