Canonical Allele Identifier: CA2673226242
Gene: CCT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10255893_10255898del , CM000667.2:g.10255893_10255898del GRCh38
NC_000005.9:g.10256005_10256010del , CM000667.1:g.10256005_10256010del GRCh37
NC_000005.8:g.10309005_10309010del NCBI36
NG_012160.1:g.10724_10729del , LRG_361:g.10724_10729del

Transcript Alleles

HGVS Amino-acid Change
ENST00000280326.9:c.332-62_332-57del MANE Select ENSP00000280326.4:n.332-62_332-57del
ENST00000280326.8:c.332-62_332-57del ENSP00000280326.4:n.332-62_332-57del
ENST00000423695.6:n.128-2218_128-2213del
ENST00000503026.5:c.269-62_269-57del ENSP00000423318.1:n.269-62_269-57del
ENST00000503454.5:c.221-62_221-57del
ENST00000506600.1:c.53-62_53-57del ENSP00000423052.1:n.53-62_53-57del
ENST00000511700.1:c.247-62_247-57del ENSP00000423087.1:n.247-62_247-57del
ENST00000512975.5:c.106-2218_106-2213del ENSP00000425751.1:n.106-2218_106-2213del
ENST00000515390.5:c.167-62_167-57del ENSP00000426923.1:n.167-62_167-57del
ENST00000515676.5:c.218-62_218-57del ENSP00000427297.1:n.218-62_218-57del
ENST00000625723.1:c.106-2218_106-2213del ENSP00000487128.1:n.106-2218_106-2213del
NM_001306153.1:c.269-62_269-57del NP_001293082.1:n.269-62_269-57del
NM_001306154.1:c.167-62_167-57del NP_001293083.1:n.167-62_167-57del
NM_001306155.1:c.53-62_53-57del NP_001293084.1:n.53-62_53-57del
NM_001306156.1:c.218-62_218-57del NP_001293085.1:n.218-62_218-57del
NM_012073.3:c.332-62_332-57del , LRG_361t1:c.332-62_332-57del NP_036205.1:n.332-62_332-57del
NM_012073.4:c.332-62_332-57del NP_036205.1:n.332-62_332-57del
NM_012073.5:c.332-62_332-57del MANE Select NP_036205.1:n.332-62_332-57del
NM_001306154.2:c.167-62_167-57del NP_001293083.1:n.167-62_167-57del
NM_001306155.2:c.53-62_53-57del NP_001293084.1:n.53-62_53-57del
NM_001306156.2:c.218-62_218-57del NP_001293085.1:n.218-62_218-57del