Canonical Allele Identifier: CA1526932811

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255980A= , CM000667.2:g.10255980A=	GRCh38
NC_000005.9:g.10256092A= , CM000667.1:g.10256092A=	GRCh37
NC_000005.8:g.10309092A=	NCBI36
NG_012160.1:g.10811A= , LRG_361:g.10811A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.357A= MANE Select	ENSP00000280326.4:p.Glu119=
ENST00000280326.8:c.357A=	ENSP00000280326.4:p.Glu119=
ENST00000423695.6:n.128-2131A=
ENST00000503026.5:c.294A=	ENSP00000423318.1:p.Glu98=
ENST00000503454.5:c.246A=
ENST00000506600.1:c.78A=	ENSP00000423052.1:p.Glu26=
ENST00000511700.1:c.272A=	ENSP00000423087.1:n.272A=
ENST00000512975.5:c.106-2131A=	ENSP00000425751.1:n.106-2131A=
ENST00000515390.5:c.192A=	ENSP00000426923.1:p.Glu64=
ENST00000515676.5:c.243A=	ENSP00000427297.1:p.Glu81=
ENST00000625723.1:c.106-2131A=	ENSP00000487128.1:n.106-2131A=
NM_001306153.1:c.294A=	NP_001293082.1:p.Glu98=
NM_001306154.1:c.192A=	NP_001293083.1:p.Glu64=
NM_001306155.1:c.78A=	NP_001293084.1:p.Glu26=
NM_001306156.1:c.243A=	NP_001293085.1:p.Glu81=
NM_012073.3:c.357A= , LRG_361t1:c.357A=	NP_036205.1:p.Glu119=
NM_012073.4:c.357A=	NP_036205.1:p.Glu119=
NM_012073.5:c.357A= MANE Select	NP_036205.1:p.Glu119=
NM_001306154.2:c.192A=	NP_001293083.1:p.Glu64=
NM_001306155.2:c.78A=	NP_001293084.1:p.Glu26=
NM_001306156.2:c.243A=	NP_001293085.1:p.Glu81=