Canonical Allele Identifier: CA1526932893

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256172T= , CM000667.2:g.10256172T=	GRCh38
NC_000005.9:g.10256284T= , CM000667.1:g.10256284T=	GRCh37
NC_000005.8:g.10309284T=	NCBI36
NG_012160.1:g.11003T= , LRG_361:g.11003T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.530+19T= MANE Select	ENSP00000280326.4:n.530+19T=
ENST00000280326.8:c.530+19T=	ENSP00000280326.4:n.530+19T=
ENST00000423695.6:n.128-1939T=
ENST00000503026.5:c.467+19T=	ENSP00000423318.1:n.467+19T=
ENST00000503454.5:c.419+19T=
ENST00000506600.1:c.251+19T=	ENSP00000423052.1:n.251+19T=
ENST00000511700.1:c.445+19T=	ENSP00000423087.1:n.445+19T=
ENST00000512975.5:c.106-1939T=	ENSP00000425751.1:n.106-1939T=
ENST00000515390.5:c.365+19T=	ENSP00000426923.1:n.365+19T=
ENST00000515676.5:c.416+19T=	ENSP00000427297.1:n.416+19T=
ENST00000625723.1:c.106-1939T=	ENSP00000487128.1:n.106-1939T=
NM_001306153.1:c.467+19T=	NP_001293082.1:n.467+19T=
NM_001306154.1:c.365+19T=	NP_001293083.1:n.365+19T=
NM_001306155.1:c.251+19T=	NP_001293084.1:n.251+19T=
NM_001306156.1:c.416+19T=	NP_001293085.1:n.416+19T=
NM_012073.3:c.530+19T= , LRG_361t1:c.530+19T=	NP_036205.1:n.530+19T=
NM_012073.4:c.530+19T=	NP_036205.1:n.530+19T=
NM_012073.5:c.530+19T= MANE Select	NP_036205.1:n.530+19T=
NM_001306154.2:c.365+19T=	NP_001293083.1:n.365+19T=
NM_001306155.2:c.251+19T=	NP_001293084.1:n.251+19T=
NM_001306156.2:c.416+19T=	NP_001293085.1:n.416+19T=