Canonical Allele Identifier: CA359725073

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233333-G-C
• MyVariant Identifiers: chr5:g.54529161G>C (hg19) ; chr5:g.55233333G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233333G>C , CM000667.2:g.55233333G>C	GRCh38
NC_000005.9:g.54529161G>C , CM000667.1:g.54529161G>C	GRCh37
NC_000005.8:g.54564918G>C	NCBI36
NG_034201.1:g.5385C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.191C>G MANE Select	ENSP00000282572.4:p.Pro64Arg
ENST00000282572.4:c.191C>G	ENSP00000282572.4:p.Pro64Arg
ENST00000501463.2:c.191C>G	ENSP00000422485.1:p.Pro64Arg
NM_021147.4:c.191C>G	NP_066970.3:p.Pro64Arg
NR_125346.1:n.385C>G
NR_125347.1:n.385C>G
NM_021147.5:c.191C>G MANE Select	NP_066970.3:p.Pro64Arg
NR_125346.2:n.276C>G
NR_125347.2:n.276C>G