Canonical Allele Identifier: CA359724921

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233310-C-G
• MyVariant Identifiers: chr5:g.54529138C>G (hg19) ; chr5:g.55233310C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233310C>G , CM000667.2:g.55233310C>G	GRCh38
NC_000005.9:g.54529138C>G , CM000667.1:g.54529138C>G	GRCh37
NC_000005.8:g.54564895C>G	NCBI36
NG_034201.1:g.5408G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.214G>C MANE Select	ENSP00000282572.4:p.Glu72Gln
ENST00000282572.4:c.214G>C	ENSP00000282572.4:p.Glu72Gln
ENST00000501463.2:c.214G>C	ENSP00000422485.1:p.Glu72Gln
NM_021147.4:c.214G>C	NP_066970.3:p.Glu72Gln
NR_125346.1:n.408G>C
NR_125347.1:n.408G>C
NM_021147.5:c.214G>C MANE Select	NP_066970.3:p.Glu72Gln
NR_125346.2:n.299G>C
NR_125347.2:n.299G>C