Canonical Allele Identifier: CA443258620

Gene: CCT5

Linked Data

• dbSNP Id: rs141821121
• MyVariant Identifiers: chr5:g.10256239A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256127A>G , CM000667.2:g.10256127A>G	GRCh38
NC_000005.9:g.10256239A>G , CM000667.1:g.10256239A>G	GRCh37
NC_000005.8:g.10309239A>G	NCBI36
NG_012160.1:g.10958A>G , LRG_361:g.10958A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.504A>G MANE Select	ENSP00000280326.4:p.Thr168=
ENST00000280326.8:c.504A>G	ENSP00000280326.4:p.Thr168=
ENST00000423695.6:n.128-1984A>G
ENST00000503026.5:c.441A>G	ENSP00000423318.1:p.Thr147=
ENST00000503454.5:c.393A>G
ENST00000506600.1:c.225A>G	ENSP00000423052.1:p.Thr75=
ENST00000511700.1:c.419A>G	ENSP00000423087.1:n.419A>G
ENST00000512975.5:c.106-1984A>G	ENSP00000425751.1:n.106-1984A>G
ENST00000515390.5:c.339A>G	ENSP00000426923.1:p.Thr113=
ENST00000515676.5:c.390A>G	ENSP00000427297.1:p.Thr130=
ENST00000625723.1:c.106-1984A>G	ENSP00000487128.1:n.106-1984A>G
NM_001306153.1:c.441A>G	NP_001293082.1:p.Thr147=
NM_001306154.1:c.339A>G	NP_001293083.1:p.Thr113=
NM_001306155.1:c.225A>G	NP_001293084.1:p.Thr75=
NM_001306156.1:c.390A>G	NP_001293085.1:p.Thr130=
NM_012073.3:c.504A>G , LRG_361t1:c.504A>G	NP_036205.1:p.Thr168=
NM_012073.4:c.504A>G	NP_036205.1:p.Thr168=
NM_012073.5:c.504A>G MANE Select	NP_036205.1:p.Thr168=
NM_001306154.2:c.339A>G	NP_001293083.1:p.Thr113=
NM_001306155.2:c.225A>G	NP_001293084.1:p.Thr75=
NM_001306156.2:c.390A>G	NP_001293085.1:p.Thr130=