Canonical Allele Identifier: CA2673856338

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232968-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232968T>C , CM000667.2:g.55232968T>C	GRCh38
NC_000005.9:g.54528796T>C , CM000667.1:g.54528796T>C	GRCh37
NC_000005.8:g.54564553T>C	NCBI36
NG_034201.1:g.5750A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+175A>G MANE Select	ENSP00000282572.4:n.381+175A>G
ENST00000282572.4:c.381+175A>G	ENSP00000282572.4:n.381+175A>G
ENST00000501463.2:c.*160A>G	ENSP00000422485.1:n.*160A>G
NM_021147.4:c.381+175A>G	NP_066970.3:n.381+175A>G
NR_125346.1:n.750A>G
NR_125347.1:n.580+170A>G
NR_125348.1:n.24A>G
NM_021147.5:c.381+175A>G MANE Select	NP_066970.3:n.381+175A>G
NR_125346.2:n.641A>G
NR_125347.2:n.471+170A>G