Canonical Allele Identifier: CA118944625

Gene: CCNO

Linked Data

• dbSNP Id: rs1001695267
• gnomAD v4: 5-55232912-C-A
• MyVariant Identifiers: chr5:g.54528740C>A (hg19) ; chr5:g.55232912C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232912C>A , CM000667.2:g.55232912C>A	GRCh38
NC_000005.9:g.54528740C>A , CM000667.1:g.54528740C>A	GRCh37
NC_000005.8:g.54564497C>A	NCBI36
NG_034201.1:g.5806G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+231G>T MANE Select	ENSP00000282572.4:n.381+231G>T
ENST00000282572.4:c.381+231G>T	ENSP00000282572.4:n.381+231G>T
ENST00000501463.2:c.*216G>T	ENSP00000422485.1:n.*216G>T
NM_021147.4:c.381+231G>T	NP_066970.3:n.381+231G>T
NR_125346.1:n.806G>T
NR_125347.1:n.580+226G>T
NR_125348.1:n.80G>T
NM_021147.5:c.381+231G>T MANE Select	NP_066970.3:n.381+231G>T
NR_125346.2:n.697G>T
NR_125347.2:n.471+226G>T