Canonical Allele Identifier: CA359721267

Gene: CCNO

Linked Data

• gnomAD v4: 5-55231674-C-T
• MyVariant Identifiers: chr5:g.54527502C>T (hg19) ; chr5:g.55231674C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231674C>T , CM000667.2:g.55231674C>T	GRCh38
NC_000005.9:g.54527502C>T , CM000667.1:g.54527502C>T	GRCh37
NC_000005.8:g.54563259C>T	NCBI36
NG_034201.1:g.7044G>A
NG_051620.1:g.642G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.754G>A MANE Select	ENSP00000282572.4:p.Ala252Thr
ENST00000282572.4:c.754G>A	ENSP00000282572.4:p.Ala252Thr
ENST00000501463.2:c.*734G>A	ENSP00000422485.1:n.*734G>A
NM_021147.4:c.754G>A	NP_066970.3:p.Ala252Thr
NR_125346.1:n.1324G>A
NR_125347.1:n.953G>A
NR_125348.1:n.818G>A
NM_021147.5:c.754G>A MANE Select	NP_066970.3:p.Ala252Thr
NR_125346.2:n.1215G>A
NR_125347.2:n.844G>A