Canonical Allele Identifier: CA2578309946

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233083_55233085del , CM000667.2:g.55233083_55233085del	GRCh38
NC_000005.9:g.54528911_54528913del , CM000667.1:g.54528911_54528913del	GRCh37
NC_000005.8:g.54564668_54564670del	NCBI36
NG_034201.1:g.5636_5638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+61_381+63del MANE Select	ENSP00000282572.4:n.381+61_381+63del
ENST00000282572.4:c.381+61_381+63del	ENSP00000282572.4:n.381+61_381+63del
ENST00000501463.2:c.*46_*48del	ENSP00000422485.1:n.*46_*48del
NM_021147.4:c.381+61_381+63del	NP_066970.3:n.381+61_381+63del
NR_125346.1:n.636_638del
NR_125347.1:n.580+56_580+58del
NM_021147.5:c.381+61_381+63del MANE Select	NP_066970.3:n.381+61_381+63del
NR_125346.2:n.527_529del
NR_125347.2:n.471+56_471+58del