Canonical Allele Identifier: CA557542332
Gene: CCT5 HGNC NCBI

Linked Data

dbSNP Id: rs1347519167

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10255923_10255935del , CM000667.2:g.10255923_10255935del GRCh38
NC_000005.9:g.10256035_10256047del , CM000667.1:g.10256035_10256047del GRCh37
NC_000005.8:g.10309035_10309047del NCBI36
NG_012160.1:g.10754_10766del , LRG_361:g.10754_10766del

Transcript Alleles

HGVS Amino-acid Change
ENST00000280326.9:c.332-32_332-20del MANE Select ENSP00000280326.4:n.332-32_332-20del
ENST00000280326.8:c.332-32_332-20del ENSP00000280326.4:n.332-32_332-20del
ENST00000423695.6:n.128-2188_128-2176del
ENST00000503026.5:c.269-32_269-20del ENSP00000423318.1:n.269-32_269-20del
ENST00000503454.5:c.221-32_221-20del
ENST00000506600.1:c.53-32_53-20del ENSP00000423052.1:n.53-32_53-20del
ENST00000511700.1:c.247-32_247-20del ENSP00000423087.1:n.247-32_247-20del
ENST00000512975.5:c.106-2188_106-2176del ENSP00000425751.1:n.106-2188_106-2176del
ENST00000515390.5:c.167-32_167-20del ENSP00000426923.1:n.167-32_167-20del
ENST00000515676.5:c.218-32_218-20del ENSP00000427297.1:n.218-32_218-20del
ENST00000625723.1:c.106-2188_106-2176del ENSP00000487128.1:n.106-2188_106-2176del
NM_001306153.1:c.269-32_269-20del NP_001293082.1:n.269-32_269-20del
NM_001306154.1:c.167-32_167-20del NP_001293083.1:n.167-32_167-20del
NM_001306155.1:c.53-32_53-20del NP_001293084.1:n.53-32_53-20del
NM_001306156.1:c.218-32_218-20del NP_001293085.1:n.218-32_218-20del
NM_012073.3:c.332-32_332-20del , LRG_361t1:c.332-32_332-20del NP_036205.1:n.332-32_332-20del
NM_012073.4:c.332-32_332-20del NP_036205.1:n.332-32_332-20del
NM_012073.5:c.332-32_332-20del MANE Select NP_036205.1:n.332-32_332-20del
NM_001306154.2:c.167-32_167-20del NP_001293083.1:n.167-32_167-20del
NM_001306155.2:c.53-32_53-20del NP_001293084.1:n.53-32_53-20del
NM_001306156.2:c.218-32_218-20del NP_001293085.1:n.218-32_218-20del