Canonical Allele Identifier: CA359725261

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233358-C-A
• MyVariant Identifiers: chr5:g.54529186C>A (hg19) ; chr5:g.55233358C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233358C>A , CM000667.2:g.55233358C>A	GRCh38
NC_000005.9:g.54529186C>A , CM000667.1:g.54529186C>A	GRCh37
NC_000005.8:g.54564943C>A	NCBI36
NG_034201.1:g.5360G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.166G>T MANE Select	ENSP00000282572.4:p.Gly56Cys
ENST00000282572.4:c.166G>T	ENSP00000282572.4:p.Gly56Cys
ENST00000501463.2:c.166G>T	ENSP00000422485.1:p.Gly56Cys
NM_021147.4:c.166G>T	NP_066970.3:p.Gly56Cys
NR_125346.1:n.360G>T
NR_125347.1:n.360G>T
NM_021147.5:c.166G>T MANE Select	NP_066970.3:p.Gly56Cys
NR_125346.2:n.251G>T
NR_125347.2:n.251G>T