Canonical Allele Identifier: CA359181552

Gene: CCT5

Linked Data

• gnomAD v4: 5-10256124-G-T
• MyVariant Identifiers: chr5:g.10256236G>T (hg19) ; chr5:g.10256124G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.501G>T MANE Select	ENSP00000280326.4:p.Gln167His
ENST00000280326.8:c.501G>T	ENSP00000280326.4:p.Gln167His
ENST00000423695.6:n.128-1987G>T
ENST00000503026.5:c.438G>T	ENSP00000423318.1:p.Gln146His
ENST00000503454.5:c.390G>T
ENST00000506600.1:c.222G>T	ENSP00000423052.1:p.Gln74His
ENST00000511700.1:c.416G>T	ENSP00000423087.1:n.416G>T
ENST00000512975.5:c.106-1987G>T	ENSP00000425751.1:n.106-1987G>T
ENST00000515390.5:c.336G>T	ENSP00000426923.1:p.Gln112His
ENST00000515676.5:c.387G>T	ENSP00000427297.1:p.Gln129His
ENST00000625723.1:c.106-1987G>T	ENSP00000487128.1:n.106-1987G>T
NM_001306153.1:c.438G>T	NP_001293082.1:p.Gln146His
NM_001306154.1:c.336G>T	NP_001293083.1:p.Gln112His
NM_001306155.1:c.222G>T	NP_001293084.1:p.Gln74His
NM_001306156.1:c.387G>T	NP_001293085.1:p.Gln129His
NM_012073.3:c.501G>T , LRG_361t1:c.501G>T	NP_036205.1:p.Gln167His
NM_012073.4:c.501G>T	NP_036205.1:p.Gln167His
NM_012073.5:c.501G>T MANE Select	NP_036205.1:p.Gln167His
NM_001306154.2:c.336G>T	NP_001293083.1:p.Gln112His
NM_001306155.2:c.222G>T	NP_001293084.1:p.Gln74His
NM_001306156.2:c.387G>T	NP_001293085.1:p.Gln129His