Canonical Allele Identifier: CA1526932881

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256139G= , CM000667.2:g.10256139G=	GRCh38
NC_000005.9:g.10256251G= , CM000667.1:g.10256251G=	GRCh37
NC_000005.8:g.10309251G=	NCBI36
NG_012160.1:g.10970G= , LRG_361:g.10970G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.516G= MANE Select	ENSP00000280326.4:p.Thr172=
ENST00000280326.8:c.516G=	ENSP00000280326.4:p.Thr172=
ENST00000423695.6:n.128-1972G=
ENST00000503026.5:c.453G=	ENSP00000423318.1:p.Thr151=
ENST00000503454.5:c.405G=
ENST00000506600.1:c.237G=	ENSP00000423052.1:p.Thr79=
ENST00000511700.1:c.431G=	ENSP00000423087.1:n.431G=
ENST00000512975.5:c.106-1972G=	ENSP00000425751.1:n.106-1972G=
ENST00000515390.5:c.351G=	ENSP00000426923.1:p.Thr117=
ENST00000515676.5:c.402G=	ENSP00000427297.1:p.Thr134=
ENST00000625723.1:c.106-1972G=	ENSP00000487128.1:n.106-1972G=
NM_001306153.1:c.453G=	NP_001293082.1:p.Thr151=
NM_001306154.1:c.351G=	NP_001293083.1:p.Thr117=
NM_001306155.1:c.237G=	NP_001293084.1:p.Thr79=
NM_001306156.1:c.402G=	NP_001293085.1:p.Thr134=
NM_012073.3:c.516G= , LRG_361t1:c.516G=	NP_036205.1:p.Thr172=
NM_012073.4:c.516G=	NP_036205.1:p.Thr172=
NM_012073.5:c.516G= MANE Select	NP_036205.1:p.Thr172=
NM_001306154.2:c.351G=	NP_001293083.1:p.Thr117=
NM_001306155.2:c.237G=	NP_001293084.1:p.Thr79=
NM_001306156.2:c.402G=	NP_001293085.1:p.Thr134=