Canonical Allele Identifier: CA1547390566

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233303G= , CM000667.2:g.55233303G=	GRCh38
NC_000005.9:g.54529131G= , CM000667.1:g.54529131G=	GRCh37
NC_000005.8:g.54564888G=	NCBI36
NG_034201.1:g.5415C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.221C= MANE Select	ENSP00000282572.4:p.Pro74=
ENST00000282572.4:c.221C=	ENSP00000282572.4:p.Pro74=
ENST00000501463.2:c.221C=	ENSP00000422485.1:p.Pro74=
NM_021147.4:c.221C=	NP_066970.3:p.Pro74=
NR_125346.1:n.415C=
NR_125347.1:n.415C=
NM_021147.5:c.221C= MANE Select	NP_066970.3:p.Pro74=
NR_125346.2:n.306C=
NR_125347.2:n.306C=