Canonical Allele Identifier: CA2673226277

Gene: CCT5

Linked Data

• dbSNP Id: rs2126503301
• gnomAD v4: 5-10256157-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256157_10256158insA , CM000667.2:g.10256157_10256158insA	GRCh38
NC_000005.9:g.10256269_10256270insA , CM000667.1:g.10256269_10256270insA	GRCh37
NC_000005.8:g.10309269_10309270insA	NCBI36
NG_012160.1:g.10988_10989insA , LRG_361:g.10988_10989insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.530+4_530+5insA MANE Select	ENSP00000280326.4:n.530+4_530+5insA
ENST00000280326.8:c.530+4_530+5insA	ENSP00000280326.4:n.530+4_530+5insA
ENST00000423695.6:n.128-1954_128-1953insA
ENST00000503026.5:c.467+4_467+5insA	ENSP00000423318.1:n.467+4_467+5insA
ENST00000503454.5:c.419+4_419+5insA
ENST00000506600.1:c.251+4_251+5insA	ENSP00000423052.1:n.251+4_251+5insA
ENST00000511700.1:c.445+4_445+5insA	ENSP00000423087.1:n.445+4_445+5insA
ENST00000512975.5:c.106-1954_106-1953insA	ENSP00000425751.1:n.106-1954_106-1953insA
ENST00000515390.5:c.365+4_365+5insA	ENSP00000426923.1:n.365+4_365+5insA
ENST00000515676.5:c.416+4_416+5insA	ENSP00000427297.1:n.416+4_416+5insA
ENST00000625723.1:c.106-1954_106-1953insA	ENSP00000487128.1:n.106-1954_106-1953insA
NM_001306153.1:c.467+4_467+5insA	NP_001293082.1:n.467+4_467+5insA
NM_001306154.1:c.365+4_365+5insA	NP_001293083.1:n.365+4_365+5insA
NM_001306155.1:c.251+4_251+5insA	NP_001293084.1:n.251+4_251+5insA
NM_001306156.1:c.416+4_416+5insA	NP_001293085.1:n.416+4_416+5insA
NM_012073.3:c.530+4_530+5insA , LRG_361t1:c.530+4_530+5insA	NP_036205.1:n.530+4_530+5insA
NM_012073.4:c.530+4_530+5insA	NP_036205.1:n.530+4_530+5insA
NM_012073.5:c.530+4_530+5insA MANE Select	NP_036205.1:n.530+4_530+5insA
NM_001306154.2:c.365+4_365+5insA	NP_001293083.1:n.365+4_365+5insA
NM_001306155.2:c.251+4_251+5insA	NP_001293084.1:n.251+4_251+5insA
NM_001306156.2:c.416+4_416+5insA	NP_001293085.1:n.416+4_416+5insA