Canonical Allele Identifier: CA443258554

Gene: CCT5

Linked Data

• gnomAD v4: 5-10256115-C-G
• MyVariant Identifiers: chr5:g.10256227C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256115C>G , CM000667.2:g.10256115C>G	GRCh38
NC_000005.9:g.10256227C>G , CM000667.1:g.10256227C>G	GRCh37
NC_000005.8:g.10309227C>G	NCBI36
NG_012160.1:g.10946C>G , LRG_361:g.10946C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.492C>G MANE Select	ENSP00000280326.4:p.Pro164=
ENST00000280326.8:c.492C>G	ENSP00000280326.4:p.Pro164=
ENST00000423695.6:n.128-1996C>G
ENST00000503026.5:c.429C>G	ENSP00000423318.1:p.Pro143=
ENST00000503454.5:c.381C>G
ENST00000506600.1:c.213C>G	ENSP00000423052.1:p.Pro71=
ENST00000511700.1:c.407C>G	ENSP00000423087.1:n.407C>G
ENST00000512975.5:c.106-1996C>G	ENSP00000425751.1:n.106-1996C>G
ENST00000515390.5:c.327C>G	ENSP00000426923.1:p.Pro109=
ENST00000515676.5:c.378C>G	ENSP00000427297.1:p.Pro126=
ENST00000625723.1:c.106-1996C>G	ENSP00000487128.1:n.106-1996C>G
NM_001306153.1:c.429C>G	NP_001293082.1:p.Pro143=
NM_001306154.1:c.327C>G	NP_001293083.1:p.Pro109=
NM_001306155.1:c.213C>G	NP_001293084.1:p.Pro71=
NM_001306156.1:c.378C>G	NP_001293085.1:p.Pro126=
NM_012073.3:c.492C>G , LRG_361t1:c.492C>G	NP_036205.1:p.Pro164=
NM_012073.4:c.492C>G	NP_036205.1:p.Pro164=
NM_012073.5:c.492C>G MANE Select	NP_036205.1:p.Pro164=
NM_001306154.2:c.327C>G	NP_001293083.1:p.Pro109=
NM_001306155.2:c.213C>G	NP_001293084.1:p.Pro71=
NM_001306156.2:c.378C>G	NP_001293085.1:p.Pro126=