Canonical Allele Identifier: CA1526932804

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255965T= , CM000667.2:g.10255965T=	GRCh38
NC_000005.9:g.10256077T= , CM000667.1:g.10256077T=	GRCh37
NC_000005.8:g.10309077T=	NCBI36
NG_012160.1:g.10796T= , LRG_361:g.10796T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280326.9:c.342T= MANE Select	ENSP00000280326.4:p.Gly114=
ENST00000280326.8:c.342T=	ENSP00000280326.4:p.Gly114=
ENST00000423695.6:n.128-2146T=
ENST00000503026.5:c.279T=	ENSP00000423318.1:p.Gly93=
ENST00000503454.5:c.231T=
ENST00000506600.1:c.63T=	ENSP00000423052.1:p.Gly21=
ENST00000511700.1:c.257T=	ENSP00000423087.1:p.Val86=
ENST00000512975.5:c.106-2146T=	ENSP00000425751.1:n.106-2146T=
ENST00000515390.5:c.177T=	ENSP00000426923.1:p.Gly59=
ENST00000515676.5:c.228T=	ENSP00000427297.1:p.Gly76=
ENST00000625723.1:c.106-2146T=	ENSP00000487128.1:n.106-2146T=
NM_001306153.1:c.279T=	NP_001293082.1:p.Gly93=
NM_001306154.1:c.177T=	NP_001293083.1:p.Gly59=
NM_001306155.1:c.63T=	NP_001293084.1:p.Gly21=
NM_001306156.1:c.228T=	NP_001293085.1:p.Gly76=
NM_012073.3:c.342T= , LRG_361t1:c.342T=	NP_036205.1:p.Gly114=
NM_012073.4:c.342T=	NP_036205.1:p.Gly114=
NM_012073.5:c.342T= MANE Select	NP_036205.1:p.Gly114=
NM_001306154.2:c.177T=	NP_001293083.1:p.Gly59=
NM_001306155.2:c.63T=	NP_001293084.1:p.Gly21=
NM_001306156.2:c.228T=	NP_001293085.1:p.Gly76=