Canonical Allele Identifier: CA443258598

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256236G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256124G>A , CM000667.2:g.10256124G>A	GRCh38
NC_000005.9:g.10256236G>A , CM000667.1:g.10256236G>A	GRCh37
NC_000005.8:g.10309236G>A	NCBI36
NG_012160.1:g.10955G>A , LRG_361:g.10955G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.501G>A MANE Select	ENSP00000280326.4:p.Gln167=
ENST00000280326.8:c.501G>A	ENSP00000280326.4:p.Gln167=
ENST00000423695.6:n.128-1987G>A
ENST00000503026.5:c.438G>A	ENSP00000423318.1:p.Gln146=
ENST00000503454.5:c.390G>A
ENST00000506600.1:c.222G>A	ENSP00000423052.1:p.Gln74=
ENST00000511700.1:c.416G>A	ENSP00000423087.1:n.416G>A
ENST00000512975.5:c.106-1987G>A	ENSP00000425751.1:n.106-1987G>A
ENST00000515390.5:c.336G>A	ENSP00000426923.1:p.Gln112=
ENST00000515676.5:c.387G>A	ENSP00000427297.1:p.Gln129=
ENST00000625723.1:c.106-1987G>A	ENSP00000487128.1:n.106-1987G>A
NM_001306153.1:c.438G>A	NP_001293082.1:p.Gln146=
NM_001306154.1:c.336G>A	NP_001293083.1:p.Gln112=
NM_001306155.1:c.222G>A	NP_001293084.1:p.Gln74=
NM_001306156.1:c.387G>A	NP_001293085.1:p.Gln129=
NM_012073.3:c.501G>A , LRG_361t1:c.501G>A	NP_036205.1:p.Gln167=
NM_012073.4:c.501G>A	NP_036205.1:p.Gln167=
NM_012073.5:c.501G>A MANE Select	NP_036205.1:p.Gln167=
NM_001306154.2:c.336G>A	NP_001293083.1:p.Gln112=
NM_001306155.2:c.222G>A	NP_001293084.1:p.Gln74=
NM_001306156.2:c.387G>A	NP_001293085.1:p.Gln129=