Canonical Allele Identifier: CA2673856296

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232924-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232924T>C , CM000667.2:g.55232924T>C	GRCh38
NC_000005.9:g.54528752T>C , CM000667.1:g.54528752T>C	GRCh37
NC_000005.8:g.54564509T>C	NCBI36
NG_034201.1:g.5794A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+219A>G MANE Select	ENSP00000282572.4:n.381+219A>G
ENST00000282572.4:c.381+219A>G	ENSP00000282572.4:n.381+219A>G
ENST00000501463.2:c.*204A>G	ENSP00000422485.1:n.*204A>G
NM_021147.4:c.381+219A>G	NP_066970.3:n.381+219A>G
NR_125346.1:n.794A>G
NR_125347.1:n.580+214A>G
NR_125348.1:n.68A>G
NM_021147.5:c.381+219A>G MANE Select	NP_066970.3:n.381+219A>G
NR_125346.2:n.685A>G
NR_125347.2:n.471+214A>G