Canonical Allele Identifier: CA1547390758

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233414A= , CM000667.2:g.55233414A=	GRCh38
NC_000005.9:g.54529242A= , CM000667.1:g.54529242A=	GRCh37
NC_000005.8:g.54564999A=	NCBI36
NG_034201.1:g.5304T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.110T= MANE Select	ENSP00000282572.4:p.Leu37=
ENST00000282572.4:c.110T=	ENSP00000282572.4:p.Leu37=
ENST00000501463.2:c.110T=	ENSP00000422485.1:p.Leu37=
NM_021147.4:c.110T=	NP_066970.3:p.Leu37=
NR_125346.1:n.304T=
NR_125347.1:n.304T=
NM_021147.5:c.110T= MANE Select	NP_066970.3:p.Leu37=
NR_125346.2:n.195T=
NR_125347.2:n.195T=