Canonical Allele Identifier: CA359721355

Gene: CCNO

Linked Data

• MyVariant Identifiers: chr5:g.54527537A>G (hg19) ; chr5:g.55231709A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231709A>G , CM000667.2:g.55231709A>G	GRCh38
NC_000005.9:g.54527537A>G , CM000667.1:g.54527537A>G	GRCh37
NC_000005.8:g.54563294A>G	NCBI36
NG_034201.1:g.7009T>C
NG_051620.1:g.607T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.719T>C MANE Select	ENSP00000282572.4:p.Phe240Ser
ENST00000282572.4:c.719T>C	ENSP00000282572.4:p.Phe240Ser
ENST00000501463.2:c.*699T>C	ENSP00000422485.1:n.*699T>C
NM_021147.4:c.719T>C	NP_066970.3:p.Phe240Ser
NR_125346.1:n.1289T>C
NR_125347.1:n.918T>C
NR_125348.1:n.783T>C
NM_021147.5:c.719T>C MANE Select	NP_066970.3:p.Phe240Ser
NR_125346.2:n.1180T>C
NR_125347.2:n.809T>C