Canonical Allele Identifier: CA1526932855

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256090T= , CM000667.2:g.10256090T=	GRCh38
NC_000005.9:g.10256202T= , CM000667.1:g.10256202T=	GRCh37
NC_000005.8:g.10309202T=	NCBI36
NG_012160.1:g.10921T= , LRG_361:g.10921T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.467T= MANE Select	ENSP00000280326.4:p.Leu156=
ENST00000280326.8:c.467T=	ENSP00000280326.4:p.Leu156=
ENST00000423695.6:n.128-2021T=
ENST00000503026.5:c.404T=	ENSP00000423318.1:p.Leu135=
ENST00000503454.5:c.356T=
ENST00000506600.1:c.188T=	ENSP00000423052.1:p.Leu63=
ENST00000511700.1:c.382T=	ENSP00000423087.1:n.382T=
ENST00000512975.5:c.106-2021T=	ENSP00000425751.1:n.106-2021T=
ENST00000515390.5:c.302T=	ENSP00000426923.1:p.Leu101=
ENST00000515676.5:c.353T=	ENSP00000427297.1:p.Leu118=
ENST00000625723.1:c.106-2021T=	ENSP00000487128.1:n.106-2021T=
NM_001306153.1:c.404T=	NP_001293082.1:p.Leu135=
NM_001306154.1:c.302T=	NP_001293083.1:p.Leu101=
NM_001306155.1:c.188T=	NP_001293084.1:p.Leu63=
NM_001306156.1:c.353T=	NP_001293085.1:p.Leu118=
NM_012073.3:c.467T= , LRG_361t1:c.467T=	NP_036205.1:p.Leu156=
NM_012073.4:c.467T=	NP_036205.1:p.Leu156=
NM_012073.5:c.467T= MANE Select	NP_036205.1:p.Leu156=
NM_001306154.2:c.302T=	NP_001293083.1:p.Leu101=
NM_001306155.2:c.188T=	NP_001293084.1:p.Leu63=
NM_001306156.2:c.353T=	NP_001293085.1:p.Leu118=