Canonical Allele Identifier: CA359721216

Gene: CCNO

Linked Data

• MyVariant Identifiers: chr5:g.54527490G>T (hg19) ; chr5:g.55231662G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231662G>T , CM000667.2:g.55231662G>T	GRCh38
NC_000005.9:g.54527490G>T , CM000667.1:g.54527490G>T	GRCh37
NC_000005.8:g.54563247G>T	NCBI36
NG_034201.1:g.7056C>A
NG_051620.1:g.654C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.766C>A MANE Select	ENSP00000282572.4:p.Leu256Met
ENST00000282572.4:c.766C>A	ENSP00000282572.4:p.Leu256Met
ENST00000501463.2:c.*746C>A	ENSP00000422485.1:n.*746C>A
NM_021147.4:c.766C>A	NP_066970.3:p.Leu256Met
NR_125346.1:n.1336C>A
NR_125347.1:n.965C>A
NR_125348.1:n.830C>A
NM_021147.5:c.766C>A MANE Select	NP_066970.3:p.Leu256Met
NR_125346.2:n.1227C>A
NR_125347.2:n.856C>A