Canonical Allele Identifier: CA359181036

Gene: CCT5

Linked Data

• gnomAD v4: 5-10255964-G-T
• MyVariant Identifiers: chr5:g.10256076G>T (hg19) ; chr5:g.10255964G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255964G>T , CM000667.2:g.10255964G>T	GRCh38
NC_000005.9:g.10256076G>T , CM000667.1:g.10256076G>T	GRCh37
NC_000005.8:g.10309076G>T	NCBI36
NG_012160.1:g.10795G>T , LRG_361:g.10795G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.341G>T MANE Select	ENSP00000280326.4:p.Gly114Val
ENST00000280326.8:c.341G>T	ENSP00000280326.4:p.Gly114Val
ENST00000423695.6:n.128-2147G>T
ENST00000503026.5:c.278G>T	ENSP00000423318.1:p.Gly93Val
ENST00000503454.5:c.230G>T
ENST00000506600.1:c.62G>T	ENSP00000423052.1:p.Gly21Val
ENST00000511700.1:c.256G>T	ENSP00000423087.1:p.Val86Leu
ENST00000512975.5:c.106-2147G>T	ENSP00000425751.1:n.106-2147G>T
ENST00000515390.5:c.176G>T	ENSP00000426923.1:p.Gly59Val
ENST00000515676.5:c.227G>T	ENSP00000427297.1:p.Gly76Val
ENST00000625723.1:c.106-2147G>T	ENSP00000487128.1:n.106-2147G>T
NM_001306153.1:c.278G>T	NP_001293082.1:p.Gly93Val
NM_001306154.1:c.176G>T	NP_001293083.1:p.Gly59Val
NM_001306155.1:c.62G>T	NP_001293084.1:p.Gly21Val
NM_001306156.1:c.227G>T	NP_001293085.1:p.Gly76Val
NM_012073.3:c.341G>T , LRG_361t1:c.341G>T	NP_036205.1:p.Gly114Val
NM_012073.4:c.341G>T	NP_036205.1:p.Gly114Val
NM_012073.5:c.341G>T MANE Select	NP_036205.1:p.Gly114Val
NM_001306154.2:c.176G>T	NP_001293083.1:p.Gly59Val
NM_001306155.2:c.62G>T	NP_001293084.1:p.Gly21Val
NM_001306156.2:c.227G>T	NP_001293085.1:p.Gly76Val