Canonical Allele Identifier: CA444396745

Gene: CCNO

Linked Data

• gnomAD v4: 5-55231708-G-A
• MyVariant Identifiers: chr5:g.54527536G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231708G>A , CM000667.2:g.55231708G>A	GRCh38
NC_000005.9:g.54527536G>A , CM000667.1:g.54527536G>A	GRCh37
NC_000005.8:g.54563293G>A	NCBI36
NG_034201.1:g.7010C>T
NG_051620.1:g.608C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.720C>T MANE Select	ENSP00000282572.4:p.Phe240=
ENST00000282572.4:c.720C>T	ENSP00000282572.4:p.Phe240=
ENST00000501463.2:c.*700C>T	ENSP00000422485.1:n.*700C>T
NM_021147.4:c.720C>T	NP_066970.3:p.Phe240=
NR_125346.1:n.1290C>T
NR_125347.1:n.919C>T
NR_125348.1:n.784C>T
NM_021147.5:c.720C>T MANE Select	NP_066970.3:p.Phe240=
NR_125346.2:n.1181C>T
NR_125347.2:n.810C>T