Canonical Allele Identifier: CA1547396615

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233053G= , CM000667.2:g.55233053G=	GRCh38
NC_000005.9:g.54528881G= , CM000667.1:g.54528881G=	GRCh37
NC_000005.8:g.54564638G=	NCBI36
NG_034201.1:g.5665C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+90C= MANE Select	ENSP00000282572.4:n.381+90C=
ENST00000282572.4:c.381+90C=	ENSP00000282572.4:n.381+90C=
ENST00000501463.2:c.*75C=	ENSP00000422485.1:n.*75C=
NM_021147.4:c.381+90C=	NP_066970.3:n.381+90C=
NR_125346.1:n.665C=
NR_125347.1:n.580+85C=
NM_021147.5:c.381+90C= MANE Select	NP_066970.3:n.381+90C=
NR_125346.2:n.556C=
NR_125347.2:n.471+85C=