Canonical Allele Identifier: CA2840264826

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255964dup , CM000667.2:g.10255964dup	GRCh38
NC_000005.9:g.10256076dup , CM000667.1:g.10256076dup	GRCh37
NC_000005.8:g.10309076dup	NCBI36
NG_012160.1:g.10795dup , LRG_361:g.10795dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.341dup MANE Select	ENSP00000280326.4:p.Ala115CysfsTer24
ENST00000280326.8:c.341dup	ENSP00000280326.4:p.Ala115CysfsTer24
ENST00000423695.6:n.128-2147dup
ENST00000503026.5:c.278dup	ENSP00000423318.1:p.Ala94CysfsTer24
ENST00000503454.5:c.230dup
ENST00000506600.1:c.62dup	ENSP00000423052.1:p.Ala22CysfsTer24
ENST00000511700.1:c.256dup	ENSP00000423087.1:p.Val86GlyfsTer?
ENST00000512975.5:c.106-2147dup	ENSP00000425751.1:n.106-2147dup
ENST00000515390.5:c.176dup	ENSP00000426923.1:p.Ala60CysfsTer24
ENST00000515676.5:c.227dup	ENSP00000427297.1:p.Ala77CysfsTer24
ENST00000625723.1:c.106-2147dup	ENSP00000487128.1:n.106-2147dup
NM_001306153.1:c.278dup	NP_001293082.1:p.Ala94CysfsTer24
NM_001306154.1:c.176dup	NP_001293083.1:p.Ala60CysfsTer24
NM_001306155.1:c.62dup	NP_001293084.1:p.Ala22CysfsTer24
NM_001306156.1:c.227dup	NP_001293085.1:p.Ala77CysfsTer24
NM_012073.3:c.341dup , LRG_361t1:c.341dup	NP_036205.1:p.Ala115CysfsTer24
NM_012073.4:c.341dup	NP_036205.1:p.Ala115CysfsTer24
NM_012073.5:c.341dup MANE Select	NP_036205.1:p.Ala115CysfsTer24
NM_001306154.2:c.176dup	NP_001293083.1:p.Ala60CysfsTer24
NM_001306155.2:c.62dup	NP_001293084.1:p.Ala22CysfsTer24
NM_001306156.2:c.227dup	NP_001293085.1:p.Ala77CysfsTer24