Canonical Allele Identifier: CA2673226274

Gene: CCT5

Linked Data

• dbSNP Id: rs2126503292
• gnomAD v4: 5-10256155-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256155_10256156insCA , CM000667.2:g.10256155_10256156insCA	GRCh38
NC_000005.9:g.10256267_10256268insCA , CM000667.1:g.10256267_10256268insCA	GRCh37
NC_000005.8:g.10309267_10309268insCA	NCBI36
NG_012160.1:g.10986_10987insCA , LRG_361:g.10986_10987insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.530+2_530+3insCA MANE Select	ENSP00000280326.4:n.530+2_530+3insCA
ENST00000280326.8:c.530+2_530+3insCA	ENSP00000280326.4:n.530+2_530+3insCA
ENST00000423695.6:n.128-1956_128-1955insCA
ENST00000503026.5:c.467+2_467+3insCA	ENSP00000423318.1:n.467+2_467+3insCA
ENST00000503454.5:c.419+2_419+3insCA
ENST00000506600.1:c.251+2_251+3insCA	ENSP00000423052.1:n.251+2_251+3insCA
ENST00000511700.1:c.445+2_445+3insCA	ENSP00000423087.1:n.445+2_445+3insCA
ENST00000512975.5:c.106-1956_106-1955insCA	ENSP00000425751.1:n.106-1956_106-1955insCA
ENST00000515390.5:c.365+2_365+3insCA	ENSP00000426923.1:n.365+2_365+3insCA
ENST00000515676.5:c.416+2_416+3insCA	ENSP00000427297.1:n.416+2_416+3insCA
ENST00000625723.1:c.106-1956_106-1955insCA	ENSP00000487128.1:n.106-1956_106-1955insCA
NM_001306153.1:c.467+2_467+3insCA	NP_001293082.1:n.467+2_467+3insCA
NM_001306154.1:c.365+2_365+3insCA	NP_001293083.1:n.365+2_365+3insCA
NM_001306155.1:c.251+2_251+3insCA	NP_001293084.1:n.251+2_251+3insCA
NM_001306156.1:c.416+2_416+3insCA	NP_001293085.1:n.416+2_416+3insCA
NM_012073.3:c.530+2_530+3insCA , LRG_361t1:c.530+2_530+3insCA	NP_036205.1:n.530+2_530+3insCA
NM_012073.4:c.530+2_530+3insCA	NP_036205.1:n.530+2_530+3insCA
NM_012073.5:c.530+2_530+3insCA MANE Select	NP_036205.1:n.530+2_530+3insCA
NM_001306154.2:c.365+2_365+3insCA	NP_001293083.1:n.365+2_365+3insCA
NM_001306155.2:c.251+2_251+3insCA	NP_001293084.1:n.251+2_251+3insCA
NM_001306156.2:c.416+2_416+3insCA	NP_001293085.1:n.416+2_416+3insCA