Canonical Allele Identifier: CA1526932837

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256050G= , CM000667.2:g.10256050G=	GRCh38
NC_000005.9:g.10256162G= , CM000667.1:g.10256162G=	GRCh37
NC_000005.8:g.10309162G=	NCBI36
NG_012160.1:g.10881G= , LRG_361:g.10881G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.427G= MANE Select	ENSP00000280326.4:p.Val143=
ENST00000280326.8:c.427G=	ENSP00000280326.4:p.Val143=
ENST00000423695.6:n.128-2061G=
ENST00000503026.5:c.364G=	ENSP00000423318.1:p.Val122=
ENST00000503454.5:c.316G=
ENST00000506600.1:c.148G=	ENSP00000423052.1:p.Val50=
ENST00000511700.1:c.342G=	ENSP00000423087.1:n.342G=
ENST00000512975.5:c.106-2061G=	ENSP00000425751.1:n.106-2061G=
ENST00000515390.5:c.262G=	ENSP00000426923.1:p.Val88=
ENST00000515676.5:c.313G=	ENSP00000427297.1:p.Val105=
ENST00000625723.1:c.106-2061G=	ENSP00000487128.1:n.106-2061G=
NM_001306153.1:c.364G=	NP_001293082.1:p.Val122=
NM_001306154.1:c.262G=	NP_001293083.1:p.Val88=
NM_001306155.1:c.148G=	NP_001293084.1:p.Val50=
NM_001306156.1:c.313G=	NP_001293085.1:p.Val105=
NM_012073.3:c.427G= , LRG_361t1:c.427G=	NP_036205.1:p.Val143=
NM_012073.4:c.427G=	NP_036205.1:p.Val143=
NM_012073.5:c.427G= MANE Select	NP_036205.1:p.Val143=
NM_001306154.2:c.262G=	NP_001293083.1:p.Val88=
NM_001306155.2:c.148G=	NP_001293084.1:p.Val50=
NM_001306156.2:c.313G=	NP_001293085.1:p.Val105=