Canonical Allele Identifier: CA1547390708

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233374C= , CM000667.2:g.55233374C=	GRCh38
NC_000005.9:g.54529202C= , CM000667.1:g.54529202C=	GRCh37
NC_000005.8:g.54564959C=	NCBI36
NG_034201.1:g.5344G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.150G= MANE Select	ENSP00000282572.4:p.Pro50=
ENST00000282572.4:c.150G=	ENSP00000282572.4:p.Pro50=
ENST00000501463.2:c.150G=	ENSP00000422485.1:p.Pro50=
NM_021147.4:c.150G=	NP_066970.3:p.Pro50=
NR_125346.1:n.344G=
NR_125347.1:n.344G=
NM_021147.5:c.150G= MANE Select	NP_066970.3:p.Pro50=
NR_125346.2:n.235G=
NR_125347.2:n.235G=