Canonical Allele Identifier: CA1547390654

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233341G= , CM000667.2:g.55233341G=	GRCh38
NC_000005.9:g.54529169G= , CM000667.1:g.54529169G=	GRCh37
NC_000005.8:g.54564926G=	NCBI36
NG_034201.1:g.5377C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.183C= MANE Select	ENSP00000282572.4:p.Phe61=
ENST00000282572.4:c.183C=	ENSP00000282572.4:p.Phe61=
ENST00000501463.2:c.183C=	ENSP00000422485.1:p.Phe61=
NM_021147.4:c.183C=	NP_066970.3:p.Phe61=
NR_125346.1:n.377C=
NR_125347.1:n.377C=
NM_021147.5:c.183C= MANE Select	NP_066970.3:p.Phe61=
NR_125346.2:n.268C=
NR_125347.2:n.268C=