Canonical Allele Identifier: CA444396855

Gene: CCNO

Linked Data

• dbSNP Id: rs1418087262
• MyVariant Identifiers: chr5:g.54527461C>T (hg19) ; chr5:g.55231633C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231633C>T , CM000667.2:g.55231633C>T	GRCh38
NC_000005.9:g.54527461C>T , CM000667.1:g.54527461C>T	GRCh37
NC_000005.8:g.54563218C>T	NCBI36
NG_034201.1:g.7085G>A
NG_051620.1:g.683G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.795G>A MANE Select	ENSP00000282572.4:p.Val265=
ENST00000282572.4:c.795G>A	ENSP00000282572.4:p.Val265=
ENST00000501463.2:c.*775G>A	ENSP00000422485.1:n.*775G>A
NM_021147.4:c.795G>A	NP_066970.3:p.Val265=
NR_125346.1:n.1365G>A
NR_125347.1:n.994G>A
NR_125348.1:n.859G>A
NM_021147.5:c.795G>A MANE Select	NP_066970.3:p.Val265=
NR_125346.2:n.1256G>A
NR_125347.2:n.885G>A