Canonical Allele Identifier: CA1547395868

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231704G= , CM000667.2:g.55231704G=	GRCh38
NC_000005.9:g.54527532G= , CM000667.1:g.54527532G=	GRCh37
NC_000005.8:g.54563289G=	NCBI36
NG_034201.1:g.7014C=
NG_051620.1:g.612C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.724C= MANE Select	ENSP00000282572.4:p.His242=
ENST00000282572.4:c.724C=	ENSP00000282572.4:p.His242=
ENST00000501463.2:c.*704C=	ENSP00000422485.1:n.*704C=
NM_021147.4:c.724C=	NP_066970.3:p.His242=
NR_125346.1:n.1294C=
NR_125347.1:n.923C=
NR_125348.1:n.788C=
NM_021147.5:c.724C= MANE Select	NP_066970.3:p.His242=
NR_125346.2:n.1185C=
NR_125347.2:n.814C=