Canonical Allele Identifier: CA359725600

Gene: CCNO

Linked Data

• dbSNP Id: rs1160723396
• MyVariant Identifiers: chr5:g.54529230T>A (hg19) ; chr5:g.55233402T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233402T>A , CM000667.2:g.55233402T>A	GRCh38
NC_000005.9:g.54529230T>A , CM000667.1:g.54529230T>A	GRCh37
NC_000005.8:g.54564987T>A	NCBI36
NG_034201.1:g.5316A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.122A>T MANE Select	ENSP00000282572.4:p.Gln41Leu
ENST00000282572.4:c.122A>T	ENSP00000282572.4:p.Gln41Leu
ENST00000501463.2:c.122A>T	ENSP00000422485.1:p.Gln41Leu
NM_021147.4:c.122A>T	NP_066970.3:p.Gln41Leu
NR_125346.1:n.316A>T
NR_125347.1:n.316A>T
NM_021147.5:c.122A>T MANE Select	NP_066970.3:p.Gln41Leu
NR_125346.2:n.207A>T
NR_125347.2:n.207A>T