Canonical Allele Identifier: CA359721324

Gene: CCNO

Linked Data

• MyVariant Identifiers: chr5:g.54527519T>G (hg19) ; chr5:g.55231691T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231691T>G , CM000667.2:g.55231691T>G	GRCh38
NC_000005.9:g.54527519T>G , CM000667.1:g.54527519T>G	GRCh37
NC_000005.8:g.54563276T>G	NCBI36
NG_034201.1:g.7027A>C
NG_051620.1:g.625A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.737A>C MANE Select	ENSP00000282572.4:p.Glu246Ala
ENST00000282572.4:c.737A>C	ENSP00000282572.4:p.Glu246Ala
ENST00000501463.2:c.*717A>C	ENSP00000422485.1:n.*717A>C
NM_021147.4:c.737A>C	NP_066970.3:p.Glu246Ala
NR_125346.1:n.1307A>C
NR_125347.1:n.936A>C
NR_125348.1:n.801A>C
NM_021147.5:c.737A>C MANE Select	NP_066970.3:p.Glu246Ala
NR_125346.2:n.1198A>C
NR_125347.2:n.827A>C