Canonical Allele Identifier: CA1526932820

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256010C= , CM000667.2:g.10256010C=	GRCh38
NC_000005.9:g.10256122C= , CM000667.1:g.10256122C=	GRCh37
NC_000005.8:g.10309122C=	NCBI36
NG_012160.1:g.10841C= , LRG_361:g.10841C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.387C= MANE Select	ENSP00000280326.4:p.His129=
ENST00000280326.8:c.387C=	ENSP00000280326.4:p.His129=
ENST00000423695.6:n.128-2101C=
ENST00000503026.5:c.324C=	ENSP00000423318.1:p.His108=
ENST00000503454.5:c.276C=
ENST00000506600.1:c.108C=	ENSP00000423052.1:p.His36=
ENST00000511700.1:c.302C=	ENSP00000423087.1:n.302C=
ENST00000512975.5:c.106-2101C=	ENSP00000425751.1:n.106-2101C=
ENST00000515390.5:c.222C=	ENSP00000426923.1:p.His74=
ENST00000515676.5:c.273C=	ENSP00000427297.1:p.His91=
ENST00000625723.1:c.106-2101C=	ENSP00000487128.1:n.106-2101C=
NM_001306153.1:c.324C=	NP_001293082.1:p.His108=
NM_001306154.1:c.222C=	NP_001293083.1:p.His74=
NM_001306155.1:c.108C=	NP_001293084.1:p.His36=
NM_001306156.1:c.273C=	NP_001293085.1:p.His91=
NM_012073.3:c.387C= , LRG_361t1:c.387C=	NP_036205.1:p.His129=
NM_012073.4:c.387C=	NP_036205.1:p.His129=
NM_012073.5:c.387C= MANE Select	NP_036205.1:p.His129=
NM_001306154.2:c.222C=	NP_001293083.1:p.His74=
NM_001306155.2:c.108C=	NP_001293084.1:p.His36=
NM_001306156.2:c.273C=	NP_001293085.1:p.His91=