Canonical Allele Identifier: CA2673226219

Gene: CCT5

Linked Data

• gnomAD v4: 5-10255860-GCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255864_10255866del , CM000667.2:g.10255864_10255866del	GRCh38
NC_000005.9:g.10255976_10255978del , CM000667.1:g.10255976_10255978del	GRCh37
NC_000005.8:g.10308976_10308978del	NCBI36
NG_012160.1:g.10695_10697del , LRG_361:g.10695_10697del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.332-91_332-89del MANE Select	ENSP00000280326.4:n.332-91_332-89del
ENST00000280326.8:c.332-91_332-89del	ENSP00000280326.4:n.332-91_332-89del
ENST00000423695.6:n.128-2247_128-2245del
ENST00000503026.5:c.269-91_269-89del	ENSP00000423318.1:n.269-91_269-89del
ENST00000503454.5:c.221-91_221-89del
ENST00000506600.1:c.53-91_53-89del	ENSP00000423052.1:n.53-91_53-89del
ENST00000511700.1:c.247-91_247-89del	ENSP00000423087.1:n.247-91_247-89del
ENST00000512975.5:c.106-2247_106-2245del	ENSP00000425751.1:n.106-2247_106-2245del
ENST00000515390.5:c.167-91_167-89del	ENSP00000426923.1:n.167-91_167-89del
ENST00000515676.5:c.218-91_218-89del	ENSP00000427297.1:n.218-91_218-89del
ENST00000625723.1:c.106-2247_106-2245del	ENSP00000487128.1:n.106-2247_106-2245del
NM_001306153.1:c.269-91_269-89del	NP_001293082.1:n.269-91_269-89del
NM_001306154.1:c.167-91_167-89del	NP_001293083.1:n.167-91_167-89del
NM_001306155.1:c.53-91_53-89del	NP_001293084.1:n.53-91_53-89del
NM_001306156.1:c.218-91_218-89del	NP_001293085.1:n.218-91_218-89del
NM_012073.3:c.332-91_332-89del , LRG_361t1:c.332-91_332-89del	NP_036205.1:n.332-91_332-89del
NM_012073.4:c.332-91_332-89del	NP_036205.1:n.332-91_332-89del
NM_012073.5:c.332-91_332-89del MANE Select	NP_036205.1:n.332-91_332-89del
NM_001306154.2:c.167-91_167-89del	NP_001293083.1:n.167-91_167-89del
NM_001306155.2:c.53-91_53-89del	NP_001293084.1:n.53-91_53-89del
NM_001306156.2:c.218-91_218-89del	NP_001293085.1:n.218-91_218-89del