Canonical Allele Identifier: CA444396667

Gene: CCNO

Linked Data

• gnomAD v4: 5-55231678-A-G
• MyVariant Identifiers: chr5:g.54527506A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231678A>G , CM000667.2:g.55231678A>G	GRCh38
NC_000005.9:g.54527506A>G , CM000667.1:g.54527506A>G	GRCh37
NC_000005.8:g.54563263A>G	NCBI36
NG_034201.1:g.7040T>C
NG_051620.1:g.638T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.750T>C MANE Select	ENSP00000282572.4:p.Ala250=
ENST00000282572.4:c.750T>C	ENSP00000282572.4:p.Ala250=
ENST00000501463.2:c.*730T>C	ENSP00000422485.1:n.*730T>C
NM_021147.4:c.750T>C	NP_066970.3:p.Ala250=
NR_125346.1:n.1320T>C
NR_125347.1:n.949T>C
NR_125348.1:n.814T>C
NM_021147.5:c.750T>C MANE Select	NP_066970.3:p.Ala250=
NR_125346.2:n.1211T>C
NR_125347.2:n.840T>C