Canonical Allele Identifier: CA359724889

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233306-C-A
• MyVariant Identifiers: chr5:g.54529134C>A (hg19) ; chr5:g.55233306C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233306C>A , CM000667.2:g.55233306C>A	GRCh38
NC_000005.9:g.54529134C>A , CM000667.1:g.54529134C>A	GRCh37
NC_000005.8:g.54564891C>A	NCBI36
NG_034201.1:g.5412G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.218G>T MANE Select	ENSP00000282572.4:p.Ser73Ile
ENST00000282572.4:c.218G>T	ENSP00000282572.4:p.Ser73Ile
ENST00000501463.2:c.218G>T	ENSP00000422485.1:p.Ser73Ile
NM_021147.4:c.218G>T	NP_066970.3:p.Ser73Ile
NR_125346.1:n.412G>T
NR_125347.1:n.412G>T
NM_021147.5:c.218G>T MANE Select	NP_066970.3:p.Ser73Ile
NR_125346.2:n.303G>T
NR_125347.2:n.303G>T