Canonical Allele Identifier: CA1547390945

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233568C= , CM000667.2:g.55233568C=	GRCh38
NC_000005.9:g.54529396C= , CM000667.1:g.54529396C=	GRCh37
NC_000005.8:g.54565153C=	NCBI36
NG_034201.1:g.5150G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.-45G= MANE Select	ENSP00000282572.4:n.-45G=
ENST00000282572.4:c.-45G=	ENSP00000282572.4:n.-45G=
ENST00000501463.2:c.-45G=	ENSP00000422485.1:n.-45G=
NM_021147.4:c.-45G=	NP_066970.3:n.-45G=
NR_125346.1:n.150G=
NR_125347.1:n.150G=
NM_021147.5:c.-45G= MANE Select	NP_066970.3:n.-45G=
NR_125346.2:n.41G=
NR_125347.2:n.41G=