Canonical Allele Identifier: CA359181077

Gene: CCT5

Linked Data

• gnomAD v4: 5-10255982-C-T
• MyVariant Identifiers: chr5:g.10256094C>T (hg19) ; chr5:g.10255982C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255982C>T , CM000667.2:g.10255982C>T	GRCh38
NC_000005.9:g.10256094C>T , CM000667.1:g.10256094C>T	GRCh37
NC_000005.8:g.10309094C>T	NCBI36
NG_012160.1:g.10813C>T , LRG_361:g.10813C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.359C>T MANE Select	ENSP00000280326.4:p.Ala120Val
ENST00000280326.8:c.359C>T	ENSP00000280326.4:p.Ala120Val
ENST00000423695.6:n.128-2129C>T
ENST00000503026.5:c.296C>T	ENSP00000423318.1:p.Ala99Val
ENST00000503454.5:c.248C>T
ENST00000506600.1:c.80C>T	ENSP00000423052.1:p.Ala27Val
ENST00000511700.1:c.274C>T	ENSP00000423087.1:n.274C>T
ENST00000512975.5:c.106-2129C>T	ENSP00000425751.1:n.106-2129C>T
ENST00000515390.5:c.194C>T	ENSP00000426923.1:p.Ala65Val
ENST00000515676.5:c.245C>T	ENSP00000427297.1:p.Ala82Val
ENST00000625723.1:c.106-2129C>T	ENSP00000487128.1:n.106-2129C>T
NM_001306153.1:c.296C>T	NP_001293082.1:p.Ala99Val
NM_001306154.1:c.194C>T	NP_001293083.1:p.Ala65Val
NM_001306155.1:c.80C>T	NP_001293084.1:p.Ala27Val
NM_001306156.1:c.245C>T	NP_001293085.1:p.Ala82Val
NM_012073.3:c.359C>T , LRG_361t1:c.359C>T	NP_036205.1:p.Ala120Val
NM_012073.4:c.359C>T	NP_036205.1:p.Ala120Val
NM_012073.5:c.359C>T MANE Select	NP_036205.1:p.Ala120Val
NM_001306154.2:c.194C>T	NP_001293083.1:p.Ala65Val
NM_001306155.2:c.80C>T	NP_001293084.1:p.Ala27Val
NM_001306156.2:c.245C>T	NP_001293085.1:p.Ala82Val