Canonical Allele Identifier: CA444396895

Gene: CCNO

Linked Data

• MyVariant Identifiers: chr5:g.54527476G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231648G>T , CM000667.2:g.55231648G>T	GRCh38
NC_000005.9:g.54527476G>T , CM000667.1:g.54527476G>T	GRCh37
NC_000005.8:g.54563233G>T	NCBI36
NG_034201.1:g.7070C>A
NG_051620.1:g.668C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.780C>A MANE Select	ENSP00000282572.4:p.Ala260=
ENST00000282572.4:c.780C>A	ENSP00000282572.4:p.Ala260=
ENST00000501463.2:c.*760C>A	ENSP00000422485.1:n.*760C>A
NM_021147.4:c.780C>A	NP_066970.3:p.Ala260=
NR_125346.1:n.1350C>A
NR_125347.1:n.979C>A
NR_125348.1:n.844C>A
NM_021147.5:c.780C>A MANE Select	NP_066970.3:p.Ala260=
NR_125346.2:n.1241C>A
NR_125347.2:n.870C>A