Canonical Allele Identifier: CA359181402
Gene: CCT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10256078G>C , CM000667.2:g.10256078G>C GRCh38
NC_000005.9:g.10256190G>C , CM000667.1:g.10256190G>C GRCh37
NC_000005.8:g.10309190G>C NCBI36
NG_012160.1:g.10909G>C , LRG_361:g.10909G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000280326.9:c.455G>C MANE Select ENSP00000280326.4:p.Ser152Thr
ENST00000280326.8:c.455G>C ENSP00000280326.4:p.Ser152Thr
ENST00000423695.6:n.128-2033G>C
ENST00000503026.5:c.392G>C ENSP00000423318.1:p.Ser131Thr
ENST00000503454.5:c.344G>C
ENST00000506600.1:c.176G>C ENSP00000423052.1:p.Ser59Thr
ENST00000511700.1:c.370G>C ENSP00000423087.1:n.370G>C
ENST00000512975.5:c.106-2033G>C ENSP00000425751.1:n.106-2033G>C
ENST00000515390.5:c.290G>C ENSP00000426923.1:p.Ser97Thr
ENST00000515676.5:c.341G>C ENSP00000427297.1:p.Ser114Thr
ENST00000625723.1:c.106-2033G>C ENSP00000487128.1:n.106-2033G>C
NM_001306153.1:c.392G>C NP_001293082.1:p.Ser131Thr
NM_001306154.1:c.290G>C NP_001293083.1:p.Ser97Thr
NM_001306155.1:c.176G>C NP_001293084.1:p.Ser59Thr
NM_001306156.1:c.341G>C NP_001293085.1:p.Ser114Thr
NM_012073.3:c.455G>C , LRG_361t1:c.455G>C NP_036205.1:p.Ser152Thr
NM_012073.4:c.455G>C NP_036205.1:p.Ser152Thr
NM_012073.5:c.455G>C MANE Select NP_036205.1:p.Ser152Thr
NM_001306154.2:c.290G>C NP_001293083.1:p.Ser97Thr
NM_001306155.2:c.176G>C NP_001293084.1:p.Ser59Thr
NM_001306156.2:c.341G>C NP_001293085.1:p.Ser114Thr