Canonical Allele Identifier: CA443258523

Gene: CCT5

Linked Data

• dbSNP Id: rs1199944427
• gnomAD v2: 5-10256218-C-T
• gnomAD v4: 5-10256106-C-T
• MyVariant Identifiers: chr5:g.10256218C>T (hg19) ; chr5:g.10256106C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256106C>T , CM000667.2:g.10256106C>T	GRCh38
NC_000005.9:g.10256218C>T , CM000667.1:g.10256218C>T	GRCh37
NC_000005.8:g.10309218C>T	NCBI36
NG_012160.1:g.10937C>T , LRG_361:g.10937C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.483C>T MANE Select	ENSP00000280326.4:p.Asp161=
ENST00000280326.8:c.483C>T	ENSP00000280326.4:p.Asp161=
ENST00000423695.6:n.128-2005C>T
ENST00000503026.5:c.420C>T	ENSP00000423318.1:p.Asp140=
ENST00000503454.5:c.372C>T
ENST00000506600.1:c.204C>T	ENSP00000423052.1:p.Asp68=
ENST00000511700.1:c.398C>T	ENSP00000423087.1:n.398C>T
ENST00000512975.5:c.106-2005C>T	ENSP00000425751.1:n.106-2005C>T
ENST00000515390.5:c.318C>T	ENSP00000426923.1:p.Asp106=
ENST00000515676.5:c.369C>T	ENSP00000427297.1:p.Asp123=
ENST00000625723.1:c.106-2005C>T	ENSP00000487128.1:n.106-2005C>T
NM_001306153.1:c.420C>T	NP_001293082.1:p.Asp140=
NM_001306154.1:c.318C>T	NP_001293083.1:p.Asp106=
NM_001306155.1:c.204C>T	NP_001293084.1:p.Asp68=
NM_001306156.1:c.369C>T	NP_001293085.1:p.Asp123=
NM_012073.3:c.483C>T , LRG_361t1:c.483C>T	NP_036205.1:p.Asp161=
NM_012073.4:c.483C>T	NP_036205.1:p.Asp161=
NM_012073.5:c.483C>T MANE Select	NP_036205.1:p.Asp161=
NM_001306154.2:c.318C>T	NP_001293083.1:p.Asp106=
NM_001306155.2:c.204C>T	NP_001293084.1:p.Asp68=
NM_001306156.2:c.369C>T	NP_001293085.1:p.Asp123=