Canonical Allele Identifier: CA2673856332

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232957-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232957C>A , CM000667.2:g.55232957C>A	GRCh38
NC_000005.9:g.54528785C>A , CM000667.1:g.54528785C>A	GRCh37
NC_000005.8:g.54564542C>A	NCBI36
NG_034201.1:g.5761G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+186G>T MANE Select	ENSP00000282572.4:n.381+186G>T
ENST00000282572.4:c.381+186G>T	ENSP00000282572.4:n.381+186G>T
ENST00000501463.2:c.*171G>T	ENSP00000422485.1:n.*171G>T
NM_021147.4:c.381+186G>T	NP_066970.3:n.381+186G>T
NR_125346.1:n.761G>T
NR_125347.1:n.580+181G>T
NR_125348.1:n.35G>T
NM_021147.5:c.381+186G>T MANE Select	NP_066970.3:n.381+186G>T
NR_125346.2:n.652G>T
NR_125347.2:n.471+181G>T