Canonical Allele Identifier: CA444397311

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233389-G-T
• MyVariant Identifiers: chr5:g.54529217G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233389G>T , CM000667.2:g.55233389G>T	GRCh38
NC_000005.9:g.54529217G>T , CM000667.1:g.54529217G>T	GRCh37
NC_000005.8:g.54564974G>T	NCBI36
NG_034201.1:g.5329C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.135C>A MANE Select	ENSP00000282572.4:p.Pro45=
ENST00000282572.4:c.135C>A	ENSP00000282572.4:p.Pro45=
ENST00000501463.2:c.135C>A	ENSP00000422485.1:p.Pro45=
NM_021147.4:c.135C>A	NP_066970.3:p.Pro45=
NR_125346.1:n.329C>A
NR_125347.1:n.329C>A
NM_021147.5:c.135C>A MANE Select	NP_066970.3:p.Pro45=
NR_125346.2:n.220C>A
NR_125347.2:n.220C>A