Canonical Allele Identifier: CA444397037

Gene: CCNO

Linked Data

• MyVariant Identifiers: chr5:g.54529136C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233308C>T , CM000667.2:g.55233308C>T	GRCh38
NC_000005.9:g.54529136C>T , CM000667.1:g.54529136C>T	GRCh37
NC_000005.8:g.54564893C>T	NCBI36
NG_034201.1:g.5410G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.216G>A MANE Select	ENSP00000282572.4:p.Glu72=
ENST00000282572.4:c.216G>A	ENSP00000282572.4:p.Glu72=
ENST00000501463.2:c.216G>A	ENSP00000422485.1:p.Glu72=
NM_021147.4:c.216G>A	NP_066970.3:p.Glu72=
NR_125346.1:n.410G>A
NR_125347.1:n.410G>A
NM_021147.5:c.216G>A MANE Select	NP_066970.3:p.Glu72=
NR_125346.2:n.301G>A
NR_125347.2:n.301G>A