Canonical Allele Identifier: CA359181575
Gene: CCT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10256132A>T , CM000667.2:g.10256132A>T GRCh38
NC_000005.9:g.10256244A>T , CM000667.1:g.10256244A>T GRCh37
NC_000005.8:g.10309244A>T NCBI36
NG_012160.1:g.10963A>T , LRG_361:g.10963A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000280326.9:c.509A>T MANE Select ENSP00000280326.4:p.Lys170Ile
ENST00000280326.8:c.509A>T ENSP00000280326.4:p.Lys170Ile
ENST00000423695.6:n.128-1979A>T
ENST00000503026.5:c.446A>T ENSP00000423318.1:p.Lys149Ile
ENST00000503454.5:c.398A>T
ENST00000506600.1:c.230A>T ENSP00000423052.1:p.Lys77Ile
ENST00000511700.1:c.424A>T ENSP00000423087.1:n.424A>T
ENST00000512975.5:c.106-1979A>T ENSP00000425751.1:n.106-1979A>T
ENST00000515390.5:c.344A>T ENSP00000426923.1:p.Lys115Ile
ENST00000515676.5:c.395A>T ENSP00000427297.1:p.Lys132Ile
ENST00000625723.1:c.106-1979A>T ENSP00000487128.1:n.106-1979A>T
NM_001306153.1:c.446A>T NP_001293082.1:p.Lys149Ile
NM_001306154.1:c.344A>T NP_001293083.1:p.Lys115Ile
NM_001306155.1:c.230A>T NP_001293084.1:p.Lys77Ile
NM_001306156.1:c.395A>T NP_001293085.1:p.Lys132Ile
NM_012073.3:c.509A>T , LRG_361t1:c.509A>T NP_036205.1:p.Lys170Ile
NM_012073.4:c.509A>T NP_036205.1:p.Lys170Ile
NM_012073.5:c.509A>T MANE Select NP_036205.1:p.Lys170Ile
NM_001306154.2:c.344A>T NP_001293083.1:p.Lys115Ile
NM_001306155.2:c.230A>T NP_001293084.1:p.Lys77Ile
NM_001306156.2:c.395A>T NP_001293085.1:p.Lys132Ile