Canonical Allele Identifier: CA359181500

Gene: CCT5

Linked Data

• dbSNP Id: rs748484897
• gnomAD v2: 5-10256219-A-T
• gnomAD v4: 5-10256107-A-T
• MyVariant Identifiers: chr5:g.10256219A>T (hg19) ; chr5:g.10256107A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256107A>T , CM000667.2:g.10256107A>T	GRCh38
NC_000005.9:g.10256219A>T , CM000667.1:g.10256219A>T	GRCh37
NC_000005.8:g.10309219A>T	NCBI36
NG_012160.1:g.10938A>T , LRG_361:g.10938A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.484A>T MANE Select	ENSP00000280326.4:p.Thr162Ser
ENST00000280326.8:c.484A>T	ENSP00000280326.4:p.Thr162Ser
ENST00000423695.6:n.128-2004A>T
ENST00000503026.5:c.421A>T	ENSP00000423318.1:p.Thr141Ser
ENST00000503454.5:c.373A>T
ENST00000506600.1:c.205A>T	ENSP00000423052.1:p.Thr69Ser
ENST00000511700.1:c.399A>T	ENSP00000423087.1:n.399A>T
ENST00000512975.5:c.106-2004A>T	ENSP00000425751.1:n.106-2004A>T
ENST00000515390.5:c.319A>T	ENSP00000426923.1:p.Thr107Ser
ENST00000515676.5:c.370A>T	ENSP00000427297.1:p.Thr124Ser
ENST00000625723.1:c.106-2004A>T	ENSP00000487128.1:n.106-2004A>T
NM_001306153.1:c.421A>T	NP_001293082.1:p.Thr141Ser
NM_001306154.1:c.319A>T	NP_001293083.1:p.Thr107Ser
NM_001306155.1:c.205A>T	NP_001293084.1:p.Thr69Ser
NM_001306156.1:c.370A>T	NP_001293085.1:p.Thr124Ser
NM_012073.3:c.484A>T , LRG_361t1:c.484A>T	NP_036205.1:p.Thr162Ser
NM_012073.4:c.484A>T	NP_036205.1:p.Thr162Ser
NM_012073.5:c.484A>T MANE Select	NP_036205.1:p.Thr162Ser
NM_001306154.2:c.319A>T	NP_001293083.1:p.Thr107Ser
NM_001306155.2:c.205A>T	NP_001293084.1:p.Thr69Ser
NM_001306156.2:c.370A>T	NP_001293085.1:p.Thr124Ser