Canonical Allele Identifier: CA1526932862

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256099T= , CM000667.2:g.10256099T=	GRCh38
NC_000005.9:g.10256211T= , CM000667.1:g.10256211T=	GRCh37
NC_000005.8:g.10309211T=	NCBI36
NG_012160.1:g.10930T= , LRG_361:g.10930T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.476T= MANE Select	ENSP00000280326.4:p.Ile159=
ENST00000280326.8:c.476T=	ENSP00000280326.4:p.Ile159=
ENST00000423695.6:n.128-2012T=
ENST00000503026.5:c.413T=	ENSP00000423318.1:p.Ile138=
ENST00000503454.5:c.365T=
ENST00000506600.1:c.197T=	ENSP00000423052.1:p.Ile66=
ENST00000511700.1:c.391T=	ENSP00000423087.1:n.391T=
ENST00000512975.5:c.106-2012T=	ENSP00000425751.1:n.106-2012T=
ENST00000515390.5:c.311T=	ENSP00000426923.1:p.Ile104=
ENST00000515676.5:c.362T=	ENSP00000427297.1:p.Ile121=
ENST00000625723.1:c.106-2012T=	ENSP00000487128.1:n.106-2012T=
NM_001306153.1:c.413T=	NP_001293082.1:p.Ile138=
NM_001306154.1:c.311T=	NP_001293083.1:p.Ile104=
NM_001306155.1:c.197T=	NP_001293084.1:p.Ile66=
NM_001306156.1:c.362T=	NP_001293085.1:p.Ile121=
NM_012073.3:c.476T= , LRG_361t1:c.476T=	NP_036205.1:p.Ile159=
NM_012073.4:c.476T=	NP_036205.1:p.Ile159=
NM_012073.5:c.476T= MANE Select	NP_036205.1:p.Ile159=
NM_001306154.2:c.311T=	NP_001293083.1:p.Ile104=
NM_001306155.2:c.197T=	NP_001293084.1:p.Ile66=
NM_001306156.2:c.362T=	NP_001293085.1:p.Ile121=