Canonical Allele Identifier: CA2673856335

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232961-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232961A>C , CM000667.2:g.55232961A>C	GRCh38
NC_000005.9:g.54528789A>C , CM000667.1:g.54528789A>C	GRCh37
NC_000005.8:g.54564546A>C	NCBI36
NG_034201.1:g.5757T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+182T>G MANE Select	ENSP00000282572.4:n.381+182T>G
ENST00000282572.4:c.381+182T>G	ENSP00000282572.4:n.381+182T>G
ENST00000501463.2:c.*167T>G	ENSP00000422485.1:n.*167T>G
NM_021147.4:c.381+182T>G	NP_066970.3:n.381+182T>G
NR_125346.1:n.757T>G
NR_125347.1:n.580+177T>G
NR_125348.1:n.31T>G
NM_021147.5:c.381+182T>G MANE Select	NP_066970.3:n.381+182T>G
NR_125346.2:n.648T>G
NR_125347.2:n.471+177T>G