Canonical Allele Identifier: CA359181630
Gene: CCT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10256150A>G , CM000667.2:g.10256150A>G GRCh38
NC_000005.9:g.10256262A>G , CM000667.1:g.10256262A>G GRCh37
NC_000005.8:g.10309262A>G NCBI36
NG_012160.1:g.10981A>G , LRG_361:g.10981A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000280326.9:c.527A>G MANE Select ENSP00000280326.4:p.Lys176Arg
ENST00000280326.8:c.527A>G ENSP00000280326.4:p.Lys176Arg
ENST00000423695.6:n.128-1961A>G
ENST00000503026.5:c.464A>G ENSP00000423318.1:p.Lys155Arg
ENST00000503454.5:c.416A>G
ENST00000506600.1:c.248A>G ENSP00000423052.1:p.Lys83Arg
ENST00000511700.1:c.442A>G ENSP00000423087.1:n.442A>G
ENST00000512975.5:c.106-1961A>G ENSP00000425751.1:n.106-1961A>G
ENST00000515390.5:c.362A>G ENSP00000426923.1:p.Lys121Arg
ENST00000515676.5:c.413A>G ENSP00000427297.1:p.Lys138Arg
ENST00000625723.1:c.106-1961A>G ENSP00000487128.1:n.106-1961A>G
NM_001306153.1:c.464A>G NP_001293082.1:p.Lys155Arg
NM_001306154.1:c.362A>G NP_001293083.1:p.Lys121Arg
NM_001306155.1:c.248A>G NP_001293084.1:p.Lys83Arg
NM_001306156.1:c.413A>G NP_001293085.1:p.Lys138Arg
NM_012073.3:c.527A>G , LRG_361t1:c.527A>G NP_036205.1:p.Lys176Arg
NM_012073.4:c.527A>G NP_036205.1:p.Lys176Arg
NM_012073.5:c.527A>G MANE Select NP_036205.1:p.Lys176Arg
NM_001306154.2:c.362A>G NP_001293083.1:p.Lys121Arg
NM_001306155.2:c.248A>G NP_001293084.1:p.Lys83Arg
NM_001306156.2:c.413A>G NP_001293085.1:p.Lys138Arg