Canonical Allele Identifier: CA2673856438

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233045-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233045C>A , CM000667.2:g.55233045C>A	GRCh38
NC_000005.9:g.54528873C>A , CM000667.1:g.54528873C>A	GRCh37
NC_000005.8:g.54564630C>A	NCBI36
NG_034201.1:g.5673G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+98G>T MANE Select	ENSP00000282572.4:n.381+98G>T
ENST00000282572.4:c.381+98G>T	ENSP00000282572.4:n.381+98G>T
ENST00000501463.2:c.*83G>T	ENSP00000422485.1:n.*83G>T
NM_021147.4:c.381+98G>T	NP_066970.3:n.381+98G>T
NR_125346.1:n.673G>T
NR_125347.1:n.580+93G>T
NM_021147.5:c.381+98G>T MANE Select	NP_066970.3:n.381+98G>T
NR_125346.2:n.564G>T
NR_125347.2:n.471+93G>T