Canonical Allele Identifier: CA1526932847

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256072A= , CM000667.2:g.10256072A=	GRCh38
NC_000005.9:g.10256184A= , CM000667.1:g.10256184A=	GRCh37
NC_000005.8:g.10309184A=	NCBI36
NG_012160.1:g.10903A= , LRG_361:g.10903A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.449A= MANE Select	ENSP00000280326.4:p.Lys150=
ENST00000280326.8:c.449A=	ENSP00000280326.4:p.Lys150=
ENST00000423695.6:n.128-2039A=
ENST00000503026.5:c.386A=	ENSP00000423318.1:p.Lys129=
ENST00000503454.5:c.338A=
ENST00000506600.1:c.170A=	ENSP00000423052.1:p.Lys57=
ENST00000511700.1:c.364A=	ENSP00000423087.1:n.364A=
ENST00000512975.5:c.106-2039A=	ENSP00000425751.1:n.106-2039A=
ENST00000515390.5:c.284A=	ENSP00000426923.1:p.Lys95=
ENST00000515676.5:c.335A=	ENSP00000427297.1:p.Lys112=
ENST00000625723.1:c.106-2039A=	ENSP00000487128.1:n.106-2039A=
NM_001306153.1:c.386A=	NP_001293082.1:p.Lys129=
NM_001306154.1:c.284A=	NP_001293083.1:p.Lys95=
NM_001306155.1:c.170A=	NP_001293084.1:p.Lys57=
NM_001306156.1:c.335A=	NP_001293085.1:p.Lys112=
NM_012073.3:c.449A= , LRG_361t1:c.449A=	NP_036205.1:p.Lys150=
NM_012073.4:c.449A=	NP_036205.1:p.Lys150=
NM_012073.5:c.449A= MANE Select	NP_036205.1:p.Lys150=
NM_001306154.2:c.284A=	NP_001293083.1:p.Lys95=
NM_001306155.2:c.170A=	NP_001293084.1:p.Lys57=
NM_001306156.2:c.335A=	NP_001293085.1:p.Lys112=