Canonical Allele Identifier: CA359181585

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256247C>G (hg19) ; chr5:g.10256135C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256135C>G , CM000667.2:g.10256135C>G	GRCh38
NC_000005.9:g.10256247C>G , CM000667.1:g.10256247C>G	GRCh37
NC_000005.8:g.10309247C>G	NCBI36
NG_012160.1:g.10966C>G , LRG_361:g.10966C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.512C>G MANE Select	ENSP00000280326.4:p.Thr171Ser
ENST00000280326.8:c.512C>G	ENSP00000280326.4:p.Thr171Ser
ENST00000423695.6:n.128-1976C>G
ENST00000503026.5:c.449C>G	ENSP00000423318.1:p.Thr150Ser
ENST00000503454.5:c.401C>G
ENST00000506600.1:c.233C>G	ENSP00000423052.1:p.Thr78Ser
ENST00000511700.1:c.427C>G	ENSP00000423087.1:n.427C>G
ENST00000512975.5:c.106-1976C>G	ENSP00000425751.1:n.106-1976C>G
ENST00000515390.5:c.347C>G	ENSP00000426923.1:p.Thr116Ser
ENST00000515676.5:c.398C>G	ENSP00000427297.1:p.Thr133Ser
ENST00000625723.1:c.106-1976C>G	ENSP00000487128.1:n.106-1976C>G
NM_001306153.1:c.449C>G	NP_001293082.1:p.Thr150Ser
NM_001306154.1:c.347C>G	NP_001293083.1:p.Thr116Ser
NM_001306155.1:c.233C>G	NP_001293084.1:p.Thr78Ser
NM_001306156.1:c.398C>G	NP_001293085.1:p.Thr133Ser
NM_012073.3:c.512C>G , LRG_361t1:c.512C>G	NP_036205.1:p.Thr171Ser
NM_012073.4:c.512C>G	NP_036205.1:p.Thr171Ser
NM_012073.5:c.512C>G MANE Select	NP_036205.1:p.Thr171Ser
NM_001306154.2:c.347C>G	NP_001293083.1:p.Thr116Ser
NM_001306155.2:c.233C>G	NP_001293084.1:p.Thr78Ser
NM_001306156.2:c.398C>G	NP_001293085.1:p.Thr133Ser