Canonical Allele Identifier: CA359181536

Gene: CCT5

Linked Data

• dbSNP Id: rs1367302402
• gnomAD v2: 5-10256231-A-G
• gnomAD v4: 5-10256119-A-G
• MyVariant Identifiers: chr5:g.10256231A>G (hg19) ; chr5:g.10256119A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256119A>G , CM000667.2:g.10256119A>G	GRCh38
NC_000005.9:g.10256231A>G , CM000667.1:g.10256231A>G	GRCh37
NC_000005.8:g.10309231A>G	NCBI36
NG_012160.1:g.10950A>G , LRG_361:g.10950A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.496A>G MANE Select	ENSP00000280326.4:p.Ile166Val
ENST00000280326.8:c.496A>G	ENSP00000280326.4:p.Ile166Val
ENST00000423695.6:n.128-1992A>G
ENST00000503026.5:c.433A>G	ENSP00000423318.1:p.Ile145Val
ENST00000503454.5:c.385A>G
ENST00000506600.1:c.217A>G	ENSP00000423052.1:p.Ile73Val
ENST00000511700.1:c.411A>G	ENSP00000423087.1:n.411A>G
ENST00000512975.5:c.106-1992A>G	ENSP00000425751.1:n.106-1992A>G
ENST00000515390.5:c.331A>G	ENSP00000426923.1:p.Ile111Val
ENST00000515676.5:c.382A>G	ENSP00000427297.1:p.Ile128Val
ENST00000625723.1:c.106-1992A>G	ENSP00000487128.1:n.106-1992A>G
NM_001306153.1:c.433A>G	NP_001293082.1:p.Ile145Val
NM_001306154.1:c.331A>G	NP_001293083.1:p.Ile111Val
NM_001306155.1:c.217A>G	NP_001293084.1:p.Ile73Val
NM_001306156.1:c.382A>G	NP_001293085.1:p.Ile128Val
NM_012073.3:c.496A>G , LRG_361t1:c.496A>G	NP_036205.1:p.Ile166Val
NM_012073.4:c.496A>G	NP_036205.1:p.Ile166Val
NM_012073.5:c.496A>G MANE Select	NP_036205.1:p.Ile166Val
NM_001306154.2:c.331A>G	NP_001293083.1:p.Ile111Val
NM_001306155.2:c.217A>G	NP_001293084.1:p.Ile73Val
NM_001306156.2:c.382A>G	NP_001293085.1:p.Ile128Val