Canonical Allele Identifier: CA1547395775

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231637C= , CM000667.2:g.55231637C=	GRCh38
NC_000005.9:g.54527465C= , CM000667.1:g.54527465C=	GRCh37
NC_000005.8:g.54563222C=	NCBI36
NG_034201.1:g.7081G=
NG_051620.1:g.679G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.791G= MANE Select	ENSP00000282572.4:p.Gly264=
ENST00000282572.4:c.791G=	ENSP00000282572.4:p.Gly264=
ENST00000501463.2:c.*771G=	ENSP00000422485.1:n.*771G=
NM_021147.4:c.791G=	NP_066970.3:p.Gly264=
NR_125346.1:n.1361G=
NR_125347.1:n.990G=
NR_125348.1:n.855G=
NM_021147.5:c.791G= MANE Select	NP_066970.3:p.Gly264=
NR_125346.2:n.1252G=
NR_125347.2:n.881G=