Canonical Allele Identifier: CA443258669

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256248C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256136C>A , CM000667.2:g.10256136C>A	GRCh38
NC_000005.9:g.10256248C>A , CM000667.1:g.10256248C>A	GRCh37
NC_000005.8:g.10309248C>A	NCBI36
NG_012160.1:g.10967C>A , LRG_361:g.10967C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.513C>A MANE Select	ENSP00000280326.4:p.Thr171=
ENST00000280326.8:c.513C>A	ENSP00000280326.4:p.Thr171=
ENST00000423695.6:n.128-1975C>A
ENST00000503026.5:c.450C>A	ENSP00000423318.1:p.Thr150=
ENST00000503454.5:c.402C>A
ENST00000506600.1:c.234C>A	ENSP00000423052.1:p.Thr78=
ENST00000511700.1:c.428C>A	ENSP00000423087.1:n.428C>A
ENST00000512975.5:c.106-1975C>A	ENSP00000425751.1:n.106-1975C>A
ENST00000515390.5:c.348C>A	ENSP00000426923.1:p.Thr116=
ENST00000515676.5:c.399C>A	ENSP00000427297.1:p.Thr133=
ENST00000625723.1:c.106-1975C>A	ENSP00000487128.1:n.106-1975C>A
NM_001306153.1:c.450C>A	NP_001293082.1:p.Thr150=
NM_001306154.1:c.348C>A	NP_001293083.1:p.Thr116=
NM_001306155.1:c.234C>A	NP_001293084.1:p.Thr78=
NM_001306156.1:c.399C>A	NP_001293085.1:p.Thr133=
NM_012073.3:c.513C>A , LRG_361t1:c.513C>A	NP_036205.1:p.Thr171=
NM_012073.4:c.513C>A	NP_036205.1:p.Thr171=
NM_012073.5:c.513C>A MANE Select	NP_036205.1:p.Thr171=
NM_001306154.2:c.348C>A	NP_001293083.1:p.Thr116=
NM_001306155.2:c.234C>A	NP_001293084.1:p.Thr78=
NM_001306156.2:c.399C>A	NP_001293085.1:p.Thr133=