Canonical Allele Identifier: CA359725132

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233341-G-T
• MyVariant Identifiers: chr5:g.54529169G>T (hg19) ; chr5:g.55233341G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233341G>T , CM000667.2:g.55233341G>T	GRCh38
NC_000005.9:g.54529169G>T , CM000667.1:g.54529169G>T	GRCh37
NC_000005.8:g.54564926G>T	NCBI36
NG_034201.1:g.5377C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.183C>A MANE Select	ENSP00000282572.4:p.Phe61Leu
ENST00000282572.4:c.183C>A	ENSP00000282572.4:p.Phe61Leu
ENST00000501463.2:c.183C>A	ENSP00000422485.1:p.Phe61Leu
NM_021147.4:c.183C>A	NP_066970.3:p.Phe61Leu
NR_125346.1:n.377C>A
NR_125347.1:n.377C>A
NM_021147.5:c.183C>A MANE Select	NP_066970.3:p.Phe61Leu
NR_125346.2:n.268C>A
NR_125347.2:n.268C>A