Canonical Allele Identifier: CA114935
Gene: CCT5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1327
dbSNP Id: rs118203986

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10256063A>G , CM000667.2:g.10256063A>G GRCh38
NC_000005.9:g.10256175A>G , CM000667.1:g.10256175A>G GRCh37
NC_000005.8:g.10309175A>G NCBI36
NG_012160.1:g.10894A>G , LRG_361:g.10894A>G

Transcript Alleles

HGVS Amino-acid change
NM_001306153.1:c.377A>G VV NP_001293082.1:p.His126Arg
NM_001306154.1:c.275A>G VV NP_001293083.1:p.His92Arg
NM_001306155.1:c.161A>G VV NP_001293084.1:p.His54Arg
NM_001306156.1:c.326A>G VV NP_001293085.1:p.His109Arg
NM_012073.3:c.440A>G , LRG_361t1:c.440A>G
NM_012073.4:c.440A>G VV NP_036205.1:p.His147Arg
NM_012073.5:c.440A>G VV MANE Preferred
ENST00000280326.8:c.440A>G ENSP00000280326.4:p.His147Arg
ENST00000423695.6:n.128-2048A>G
ENST00000503026.5:c.377A>G ENSP00000423318.1:p.His126Arg
ENST00000503454.5:n.329A>G
ENST00000506600.1:c.161A>G ENSP00000423052.1:p.His54Arg
ENST00000511700.1:n.355A>G ENSP00000423087.1:p.=
ENST00000512975.5:c.106-2048A>G ENSP00000425751.1:p.=
ENST00000515390.5:c.275A>G ENSP00000426923.1:p.His92Arg
ENST00000515676.5:c.326A>G ENSP00000427297.1:p.His109Arg
ENST00000625723.1:n.106-2048A>G ENSP00000487128.1:p.=