Canonical Allele Identifier: CA3198049
Gene: CCT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1634156
ClinVar RCV Id: RCV002124378
dbSNP Id: rs376551309

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10255936_10255939del , CM000667.2:g.10255936_10255939del GRCh38
NC_000005.9:g.10256048_10256051del , CM000667.1:g.10256048_10256051del GRCh37
NC_000005.8:g.10309048_10309051del NCBI36
NG_012160.1:g.10767_10770del , LRG_361:g.10767_10770del

Transcript Alleles

HGVS Amino-acid Change
ENST00000280326.9:c.332-19_332-16del MANE Select ENSP00000280326.4:n.332-19_332-16del
ENST00000280326.8:c.332-19_332-16del ENSP00000280326.4:n.332-19_332-16del
ENST00000423695.6:n.128-2175_128-2172del
ENST00000503026.5:c.269-19_269-16del ENSP00000423318.1:n.269-19_269-16del
ENST00000503454.5:c.221-19_221-16del
ENST00000506600.1:c.53-19_53-16del ENSP00000423052.1:n.53-19_53-16del
ENST00000511700.1:c.247-19_247-16del ENSP00000423087.1:n.247-19_247-16del
ENST00000512975.5:c.106-2175_106-2172del ENSP00000425751.1:n.106-2175_106-2172del
ENST00000515390.5:c.167-19_167-16del ENSP00000426923.1:n.167-19_167-16del
ENST00000515676.5:c.218-19_218-16del ENSP00000427297.1:n.218-19_218-16del
ENST00000625723.1:c.106-2175_106-2172del ENSP00000487128.1:n.106-2175_106-2172del
NM_001306153.1:c.269-19_269-16del NP_001293082.1:n.269-19_269-16del
NM_001306154.1:c.167-19_167-16del NP_001293083.1:n.167-19_167-16del
NM_001306155.1:c.53-19_53-16del NP_001293084.1:n.53-19_53-16del
NM_001306156.1:c.218-19_218-16del NP_001293085.1:n.218-19_218-16del
NM_012073.3:c.332-19_332-16del , LRG_361t1:c.332-19_332-16del NP_036205.1:n.332-19_332-16del
NM_012073.4:c.332-19_332-16del NP_036205.1:n.332-19_332-16del
NM_012073.5:c.332-19_332-16del MANE Select NP_036205.1:n.332-19_332-16del
NM_001306154.2:c.167-19_167-16del NP_001293083.1:n.167-19_167-16del
NM_001306155.2:c.53-19_53-16del NP_001293084.1:n.53-19_53-16del
NM_001306156.2:c.218-19_218-16del NP_001293085.1:n.218-19_218-16del