Canonical Allele Identifier: CA359181525

Gene: CCT5

Linked Data

• dbSNP Id: rs771088141
• gnomAD v2: 5-10256226-C-T
• gnomAD v4: 5-10256114-C-T
• MyVariant Identifiers: chr5:g.10256226C>T (hg19) ; chr5:g.10256114C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256114C>T , CM000667.2:g.10256114C>T	GRCh38
NC_000005.9:g.10256226C>T , CM000667.1:g.10256226C>T	GRCh37
NC_000005.8:g.10309226C>T	NCBI36
NG_012160.1:g.10945C>T , LRG_361:g.10945C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.491C>T MANE Select	ENSP00000280326.4:p.Pro164Leu
ENST00000280326.8:c.491C>T	ENSP00000280326.4:p.Pro164Leu
ENST00000423695.6:n.128-1997C>T
ENST00000503026.5:c.428C>T	ENSP00000423318.1:p.Pro143Leu
ENST00000503454.5:c.380C>T
ENST00000506600.1:c.212C>T	ENSP00000423052.1:p.Pro71Leu
ENST00000511700.1:c.406C>T	ENSP00000423087.1:n.406C>T
ENST00000512975.5:c.106-1997C>T	ENSP00000425751.1:n.106-1997C>T
ENST00000515390.5:c.326C>T	ENSP00000426923.1:p.Pro109Leu
ENST00000515676.5:c.377C>T	ENSP00000427297.1:p.Pro126Leu
ENST00000625723.1:c.106-1997C>T	ENSP00000487128.1:n.106-1997C>T
NM_001306153.1:c.428C>T	NP_001293082.1:p.Pro143Leu
NM_001306154.1:c.326C>T	NP_001293083.1:p.Pro109Leu
NM_001306155.1:c.212C>T	NP_001293084.1:p.Pro71Leu
NM_001306156.1:c.377C>T	NP_001293085.1:p.Pro126Leu
NM_012073.3:c.491C>T , LRG_361t1:c.491C>T	NP_036205.1:p.Pro164Leu
NM_012073.4:c.491C>T	NP_036205.1:p.Pro164Leu
NM_012073.5:c.491C>T MANE Select	NP_036205.1:p.Pro164Leu
NM_001306154.2:c.326C>T	NP_001293083.1:p.Pro109Leu
NM_001306155.2:c.212C>T	NP_001293084.1:p.Pro71Leu
NM_001306156.2:c.377C>T	NP_001293085.1:p.Pro126Leu