Canonical Allele Identifier: CA2673856346

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232975-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232975G>C , CM000667.2:g.55232975G>C	GRCh38
NC_000005.9:g.54528803G>C , CM000667.1:g.54528803G>C	GRCh37
NC_000005.8:g.54564560G>C	NCBI36
NG_034201.1:g.5743C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+168C>G MANE Select	ENSP00000282572.4:n.381+168C>G
ENST00000282572.4:c.381+168C>G	ENSP00000282572.4:n.381+168C>G
ENST00000501463.2:c.*153C>G	ENSP00000422485.1:n.*153C>G
NM_021147.4:c.381+168C>G	NP_066970.3:n.381+168C>G
NR_125346.1:n.743C>G
NR_125347.1:n.580+163C>G
NR_125348.1:n.17C>G
NM_021147.5:c.381+168C>G MANE Select	NP_066970.3:n.381+168C>G
NR_125346.2:n.634C>G
NR_125347.2:n.471+163C>G