Canonical Allele Identifier: CA444396824

Gene: CCNO

Linked Data

• gnomAD v4: 5-55231621-A-G
• MyVariant Identifiers: chr5:g.54527449A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231621A>G , CM000667.2:g.55231621A>G	GRCh38
NC_000005.9:g.54527449A>G , CM000667.1:g.54527449A>G	GRCh37
NC_000005.8:g.54563206A>G	NCBI36
NG_034201.1:g.7097T>C
NG_051620.1:g.695T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.807T>C MANE Select	ENSP00000282572.4:p.Ser269=
ENST00000282572.4:c.807T>C	ENSP00000282572.4:p.Ser269=
ENST00000501463.2:c.*787T>C	ENSP00000422485.1:n.*787T>C
NM_021147.4:c.807T>C	NP_066970.3:p.Ser269=
NR_125346.1:n.1377T>C
NR_125347.1:n.1006T>C
NR_125348.1:n.871T>C
NM_021147.5:c.807T>C MANE Select	NP_066970.3:p.Ser269=
NR_125346.2:n.1268T>C
NR_125347.2:n.897T>C