Canonical Allele Identifier: CA2673856328

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232955-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232955_55232956insCG , CM000667.2:g.55232955_55232956insCG	GRCh38
NC_000005.9:g.54528783_54528784insCG , CM000667.1:g.54528783_54528784insCG	GRCh37
NC_000005.8:g.54564540_54564541insCG	NCBI36
NG_034201.1:g.5762_5763insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+187_381+188insCG MANE Select	ENSP00000282572.4:n.381+187_381+188insCG
ENST00000282572.4:c.381+187_381+188insCG	ENSP00000282572.4:n.381+187_381+188insCG
ENST00000501463.2:c.*172_*173insCG	ENSP00000422485.1:n.*172_*173insCG
NM_021147.4:c.381+187_381+188insCG	NP_066970.3:n.381+187_381+188insCG
NR_125346.1:n.762_763insCG
NR_125347.1:n.580+182_580+183insCG
NR_125348.1:n.36_37insCG
NM_021147.5:c.381+187_381+188insCG MANE Select	NP_066970.3:n.381+187_381+188insCG
NR_125346.2:n.653_654insCG
NR_125347.2:n.471+182_471+183insCG