Canonical Allele Identifier: CA1526932806

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255970T= , CM000667.2:g.10255970T=	GRCh38
NC_000005.9:g.10256082T= , CM000667.1:g.10256082T=	GRCh37
NC_000005.8:g.10309082T=	NCBI36
NG_012160.1:g.10801T= , LRG_361:g.10801T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.347T= MANE Select	ENSP00000280326.4:p.Leu116=
ENST00000280326.8:c.347T=	ENSP00000280326.4:p.Leu116=
ENST00000423695.6:n.128-2141T=
ENST00000503026.5:c.284T=	ENSP00000423318.1:p.Leu95=
ENST00000503454.5:c.236T=
ENST00000506600.1:c.68T=	ENSP00000423052.1:p.Leu23=
ENST00000511700.1:c.262T=	ENSP00000423087.1:p.Cys88=
ENST00000512975.5:c.106-2141T=	ENSP00000425751.1:n.106-2141T=
ENST00000515390.5:c.182T=	ENSP00000426923.1:p.Leu61=
ENST00000515676.5:c.233T=	ENSP00000427297.1:p.Leu78=
ENST00000625723.1:c.106-2141T=	ENSP00000487128.1:n.106-2141T=
NM_001306153.1:c.284T=	NP_001293082.1:p.Leu95=
NM_001306154.1:c.182T=	NP_001293083.1:p.Leu61=
NM_001306155.1:c.68T=	NP_001293084.1:p.Leu23=
NM_001306156.1:c.233T=	NP_001293085.1:p.Leu78=
NM_012073.3:c.347T= , LRG_361t1:c.347T=	NP_036205.1:p.Leu116=
NM_012073.4:c.347T=	NP_036205.1:p.Leu116=
NM_012073.5:c.347T= MANE Select	NP_036205.1:p.Leu116=
NM_001306154.2:c.182T=	NP_001293083.1:p.Leu61=
NM_001306155.2:c.68T=	NP_001293084.1:p.Leu23=
NM_001306156.2:c.233T=	NP_001293085.1:p.Leu78=