Canonical Allele Identifier: CA1526932840

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256059G= , CM000667.2:g.10256059G=	GRCh38
NC_000005.9:g.10256171G= , CM000667.1:g.10256171G=	GRCh37
NC_000005.8:g.10309171G=	NCBI36
NG_012160.1:g.10890G= , LRG_361:g.10890G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.436G= MANE Select	ENSP00000280326.4:p.Glu146=
ENST00000280326.8:c.436G=	ENSP00000280326.4:p.Glu146=
ENST00000423695.6:n.128-2052G=
ENST00000503026.5:c.373G=	ENSP00000423318.1:p.Glu125=
ENST00000503454.5:c.325G=
ENST00000506600.1:c.157G=	ENSP00000423052.1:p.Glu53=
ENST00000511700.1:c.351G=	ENSP00000423087.1:n.351G=
ENST00000512975.5:c.106-2052G=	ENSP00000425751.1:n.106-2052G=
ENST00000515390.5:c.271G=	ENSP00000426923.1:p.Glu91=
ENST00000515676.5:c.322G=	ENSP00000427297.1:p.Glu108=
ENST00000625723.1:c.106-2052G=	ENSP00000487128.1:n.106-2052G=
NM_001306153.1:c.373G=	NP_001293082.1:p.Glu125=
NM_001306154.1:c.271G=	NP_001293083.1:p.Glu91=
NM_001306155.1:c.157G=	NP_001293084.1:p.Glu53=
NM_001306156.1:c.322G=	NP_001293085.1:p.Glu108=
NM_012073.3:c.436G= , LRG_361t1:c.436G=	NP_036205.1:p.Glu146=
NM_012073.4:c.436G=	NP_036205.1:p.Glu146=
NM_012073.5:c.436G= MANE Select	NP_036205.1:p.Glu146=
NM_001306154.2:c.271G=	NP_001293083.1:p.Glu91=
NM_001306155.2:c.157G=	NP_001293084.1:p.Glu53=
NM_001306156.2:c.322G=	NP_001293085.1:p.Glu108=