Canonical Allele Identifier: CA1526932879

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256131A= , CM000667.2:g.10256131A=	GRCh38
NC_000005.9:g.10256243A= , CM000667.1:g.10256243A=	GRCh37
NC_000005.8:g.10309243A=	NCBI36
NG_012160.1:g.10962A= , LRG_361:g.10962A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.508A= MANE Select	ENSP00000280326.4:p.Lys170=
ENST00000280326.8:c.508A=	ENSP00000280326.4:p.Lys170=
ENST00000423695.6:n.128-1980A=
ENST00000503026.5:c.445A=	ENSP00000423318.1:p.Lys149=
ENST00000503454.5:c.397A=
ENST00000506600.1:c.229A=	ENSP00000423052.1:p.Lys77=
ENST00000511700.1:c.423A=	ENSP00000423087.1:n.423A=
ENST00000512975.5:c.106-1980A=	ENSP00000425751.1:n.106-1980A=
ENST00000515390.5:c.343A=	ENSP00000426923.1:p.Lys115=
ENST00000515676.5:c.394A=	ENSP00000427297.1:p.Lys132=
ENST00000625723.1:c.106-1980A=	ENSP00000487128.1:n.106-1980A=
NM_001306153.1:c.445A=	NP_001293082.1:p.Lys149=
NM_001306154.1:c.343A=	NP_001293083.1:p.Lys115=
NM_001306155.1:c.229A=	NP_001293084.1:p.Lys77=
NM_001306156.1:c.394A=	NP_001293085.1:p.Lys132=
NM_012073.3:c.508A= , LRG_361t1:c.508A=	NP_036205.1:p.Lys170=
NM_012073.4:c.508A=	NP_036205.1:p.Lys170=
NM_012073.5:c.508A= MANE Select	NP_036205.1:p.Lys170=
NM_001306154.2:c.343A=	NP_001293083.1:p.Lys115=
NM_001306155.2:c.229A=	NP_001293084.1:p.Lys77=
NM_001306156.2:c.394A=	NP_001293085.1:p.Lys132=