Canonical Allele Identifier: CA359725172

Gene: CCNO

Linked Data

• MyVariant Identifiers: chr5:g.54529173A>T (hg19) ; chr5:g.55233345A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233345A>T , CM000667.2:g.55233345A>T	GRCh38
NC_000005.9:g.54529173A>T , CM000667.1:g.54529173A>T	GRCh37
NC_000005.8:g.54564930A>T	NCBI36
NG_034201.1:g.5373T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.179T>A MANE Select	ENSP00000282572.4:p.Leu60Gln
ENST00000282572.4:c.179T>A	ENSP00000282572.4:p.Leu60Gln
ENST00000501463.2:c.179T>A	ENSP00000422485.1:p.Leu60Gln
NM_021147.4:c.179T>A	NP_066970.3:p.Leu60Gln
NR_125346.1:n.373T>A
NR_125347.1:n.373T>A
NM_021147.5:c.179T>A MANE Select	NP_066970.3:p.Leu60Gln
NR_125346.2:n.264T>A
NR_125347.2:n.264T>A