Canonical Allele Identifier: CA2597387230

Gene: CCNO

Linked Data

• gnomAD v3: 5-55233002-A-C
• gnomAD v4: 5-55233002-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233002A>C , CM000667.2:g.55233002A>C	GRCh38
NC_000005.9:g.54528830A>C , CM000667.1:g.54528830A>C	GRCh37
NC_000005.8:g.54564587A>C	NCBI36
NG_034201.1:g.5716T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+141T>G MANE Select	ENSP00000282572.4:n.381+141T>G
ENST00000282572.4:c.381+141T>G	ENSP00000282572.4:n.381+141T>G
ENST00000501463.2:c.*126T>G	ENSP00000422485.1:n.*126T>G
NM_021147.4:c.381+141T>G	NP_066970.3:n.381+141T>G
NR_125346.1:n.716T>G
NR_125347.1:n.580+136T>G
NM_021147.5:c.381+141T>G MANE Select	NP_066970.3:n.381+141T>G
NR_125346.2:n.607T>G
NR_125347.2:n.471+136T>G