Canonical Allele Identifier: CA1526932857

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256092G= , CM000667.2:g.10256092G=	GRCh38
NC_000005.9:g.10256204G= , CM000667.1:g.10256204G=	GRCh37
NC_000005.8:g.10309204G=	NCBI36
NG_012160.1:g.10923G= , LRG_361:g.10923G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.469G= MANE Select	ENSP00000280326.4:p.Val157=
ENST00000280326.8:c.469G=	ENSP00000280326.4:p.Val157=
ENST00000423695.6:n.128-2019G=
ENST00000503026.5:c.406G=	ENSP00000423318.1:p.Val136=
ENST00000503454.5:c.358G=
ENST00000506600.1:c.190G=	ENSP00000423052.1:p.Val64=
ENST00000511700.1:c.384G=	ENSP00000423087.1:n.384G=
ENST00000512975.5:c.106-2019G=	ENSP00000425751.1:n.106-2019G=
ENST00000515390.5:c.304G=	ENSP00000426923.1:p.Val102=
ENST00000515676.5:c.355G=	ENSP00000427297.1:p.Val119=
ENST00000625723.1:c.106-2019G=	ENSP00000487128.1:n.106-2019G=
NM_001306153.1:c.406G=	NP_001293082.1:p.Val136=
NM_001306154.1:c.304G=	NP_001293083.1:p.Val102=
NM_001306155.1:c.190G=	NP_001293084.1:p.Val64=
NM_001306156.1:c.355G=	NP_001293085.1:p.Val119=
NM_012073.3:c.469G= , LRG_361t1:c.469G=	NP_036205.1:p.Val157=
NM_012073.4:c.469G=	NP_036205.1:p.Val157=
NM_012073.5:c.469G= MANE Select	NP_036205.1:p.Val157=
NM_001306154.2:c.304G=	NP_001293083.1:p.Val102=
NM_001306155.2:c.190G=	NP_001293084.1:p.Val64=
NM_001306156.2:c.355G=	NP_001293085.1:p.Val119=