Canonical Allele Identifier: CA1526932842

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256063A= , CM000667.2:g.10256063A=	GRCh38
NC_000005.9:g.10256175A= , CM000667.1:g.10256175A=	GRCh37
NC_000005.8:g.10309175A=	NCBI36
NG_012160.1:g.10894A= , LRG_361:g.10894A=

Transcript Alleles

HGVS	Amino-acid Change
NM_012073.5:c.440A= MANE Select	NP_036205.1:p.His147=
ENST00000280326.9:c.440A= MANE Select	ENSP00000280326.4:p.His147=
NM_001306153.1:c.377A=	NP_001293082.1:p.His126=
NM_001306154.1:c.275A=	NP_001293083.1:p.His92=
NM_001306154.2:c.275A=	NP_001293083.1:p.His92=
NM_001306155.1:c.161A=	NP_001293084.1:p.His54=
NM_001306155.2:c.161A=	NP_001293084.1:p.His54=
NM_001306156.1:c.326A=	NP_001293085.1:p.His109=
NM_001306156.2:c.326A=	NP_001293085.1:p.His109=
NM_012073.3:c.440A= , LRG_361t1:c.440A=	NP_036205.1:p.His147=
NM_012073.4:c.440A=	NP_036205.1:p.His147=
ENST00000280326.8:c.440A=	ENSP00000280326.4:p.His147=
ENST00000423695.6:n.128-2048A=
ENST00000503026.5:c.377A=	ENSP00000423318.1:p.His126=
ENST00000503454.5:c.329A=
ENST00000506600.1:c.161A=	ENSP00000423052.1:p.His54=
ENST00000511700.1:c.355A=	ENSP00000423087.1:n.355A=
ENST00000512975.5:c.106-2048A=	ENSP00000425751.1:n.106-2048A=
ENST00000515390.5:c.275A=	ENSP00000426923.1:p.His92=
ENST00000515676.5:c.326A=	ENSP00000427297.1:p.His109=
ENST00000625723.1:c.106-2048A=	ENSP00000487128.1:n.106-2048A=