Canonical Allele Identifier: CA1526932877

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256122C= , CM000667.2:g.10256122C=	GRCh38
NC_000005.9:g.10256234C= , CM000667.1:g.10256234C=	GRCh37
NC_000005.8:g.10309234C=	NCBI36
NG_012160.1:g.10953C= , LRG_361:g.10953C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.499C= MANE Select	ENSP00000280326.4:p.Gln167=
ENST00000280326.8:c.499C=	ENSP00000280326.4:p.Gln167=
ENST00000423695.6:n.128-1989C=
ENST00000503026.5:c.436C=	ENSP00000423318.1:p.Gln146=
ENST00000503454.5:c.388C=
ENST00000506600.1:c.220C=	ENSP00000423052.1:p.Gln74=
ENST00000511700.1:c.414C=	ENSP00000423087.1:n.414C=
ENST00000512975.5:c.106-1989C=	ENSP00000425751.1:n.106-1989C=
ENST00000515390.5:c.334C=	ENSP00000426923.1:p.Gln112=
ENST00000515676.5:c.385C=	ENSP00000427297.1:p.Gln129=
ENST00000625723.1:c.106-1989C=	ENSP00000487128.1:n.106-1989C=
NM_001306153.1:c.436C=	NP_001293082.1:p.Gln146=
NM_001306154.1:c.334C=	NP_001293083.1:p.Gln112=
NM_001306155.1:c.220C=	NP_001293084.1:p.Gln74=
NM_001306156.1:c.385C=	NP_001293085.1:p.Gln129=
NM_012073.3:c.499C= , LRG_361t1:c.499C=	NP_036205.1:p.Gln167=
NM_012073.4:c.499C=	NP_036205.1:p.Gln167=
NM_012073.5:c.499C= MANE Select	NP_036205.1:p.Gln167=
NM_001306154.2:c.334C=	NP_001293083.1:p.Gln112=
NM_001306155.2:c.220C=	NP_001293084.1:p.Gln74=
NM_001306156.2:c.385C=	NP_001293085.1:p.Gln129=