Canonical Allele Identifier: CA359724052

Gene: CCNO

Linked Data

• MyVariant Identifiers: chr5:g.54529005A>T (hg19) ; chr5:g.55233177A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233177A>T , CM000667.2:g.55233177A>T	GRCh38
NC_000005.9:g.54529005A>T , CM000667.1:g.54529005A>T	GRCh37
NC_000005.8:g.54564762A>T	NCBI36
NG_034201.1:g.5541T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.347T>A MANE Select	ENSP00000282572.4:p.Phe116Tyr
ENST00000282572.4:c.347T>A	ENSP00000282572.4:p.Phe116Tyr
ENST00000501463.2:c.347T>A	ENSP00000422485.1:p.Phe116Tyr
NM_021147.4:c.347T>A	NP_066970.3:p.Phe116Tyr
NR_125346.1:n.541T>A
NR_125347.1:n.541T>A
NM_021147.5:c.347T>A MANE Select	NP_066970.3:p.Phe116Tyr
NR_125346.2:n.432T>A
NR_125347.2:n.432T>A