Canonical Allele Identifier: CA1526932880

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256138C= , CM000667.2:g.10256138C=	GRCh38
NC_000005.9:g.10256250C= , CM000667.1:g.10256250C=	GRCh37
NC_000005.8:g.10309250C=	NCBI36
NG_012160.1:g.10969C= , LRG_361:g.10969C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.515C= MANE Select	ENSP00000280326.4:p.Thr172=
ENST00000280326.8:c.515C=	ENSP00000280326.4:p.Thr172=
ENST00000423695.6:n.128-1973C=
ENST00000503026.5:c.452C=	ENSP00000423318.1:p.Thr151=
ENST00000503454.5:c.404C=
ENST00000506600.1:c.236C=	ENSP00000423052.1:p.Thr79=
ENST00000511700.1:c.430C=	ENSP00000423087.1:n.430C=
ENST00000512975.5:c.106-1973C=	ENSP00000425751.1:n.106-1973C=
ENST00000515390.5:c.350C=	ENSP00000426923.1:p.Thr117=
ENST00000515676.5:c.401C=	ENSP00000427297.1:p.Thr134=
ENST00000625723.1:c.106-1973C=	ENSP00000487128.1:n.106-1973C=
NM_001306153.1:c.452C=	NP_001293082.1:p.Thr151=
NM_001306154.1:c.350C=	NP_001293083.1:p.Thr117=
NM_001306155.1:c.236C=	NP_001293084.1:p.Thr79=
NM_001306156.1:c.401C=	NP_001293085.1:p.Thr134=
NM_012073.3:c.515C= , LRG_361t1:c.515C=	NP_036205.1:p.Thr172=
NM_012073.4:c.515C=	NP_036205.1:p.Thr172=
NM_012073.5:c.515C= MANE Select	NP_036205.1:p.Thr172=
NM_001306154.2:c.350C=	NP_001293083.1:p.Thr117=
NM_001306155.2:c.236C=	NP_001293084.1:p.Thr79=
NM_001306156.2:c.401C=	NP_001293085.1:p.Thr134=