Canonical Allele Identifier: CA118944770

Gene: CCNO

Linked Data

• dbSNP Id: rs538223997
• MyVariant Identifiers: chr5:g.54528892_54528893insA (hg19) ; chr5:g.55233064_55233065insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233064_55233065insA , CM000667.2:g.55233064_55233065insA	GRCh38
NC_000005.9:g.54528892_54528893insA , CM000667.1:g.54528892_54528893insA	GRCh37
NC_000005.8:g.54564649_54564650insA	NCBI36
NG_034201.1:g.5653_5654insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+78_381+79insT MANE Select	ENSP00000282572.4:n.381+78_381+79insT
ENST00000282572.4:c.381+78_381+79insT	ENSP00000282572.4:n.381+78_381+79insT
ENST00000501463.2:c.*63_*64insT	ENSP00000422485.1:n.*63_*64insT
NM_021147.4:c.381+78_381+79insT	NP_066970.3:n.381+78_381+79insT
NR_125346.1:n.653_654insT
NR_125347.1:n.580+73_580+74insT
NM_021147.5:c.381+78_381+79insT MANE Select	NP_066970.3:n.381+78_381+79insT
NR_125346.2:n.544_545insT
NR_125347.2:n.471+73_471+74insT