Canonical Allele Identifier: CA10618733

Gene: CCT5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10266160C>G , CM000667.2:g.10266160C>G	GRCh38
NC_000005.9:g.10266272C>G , CM000667.1:g.10266272C>G	GRCh37
NC_000005.8:g.10319272C>G	NCBI36
NG_012160.1:g.20991C>G , LRG_361:g.20991C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_012073.5:c.*1377C>G MANE Select	NP_036205.1:n.*1377C>G
ENST00000280326.9:c.*1377C>G MANE Select	ENSP00000280326.4:n.*1377C>G
NM_001306153.1:c.*1377C>G	NP_001293082.1:n.*1377C>G
NM_001306154.1:c.*1377C>G	NP_001293083.1:n.*1377C>G
NM_001306154.2:c.*1377C>G	NP_001293083.1:n.*1377C>G
NM_001306155.1:c.*1377C>G	NP_001293084.1:n.*1377C>G
NM_001306155.2:c.*1377C>G	NP_001293084.1:n.*1377C>G
NM_001306156.1:c.*1377C>G	NP_001293085.1:n.*1377C>G
NM_001306156.2:c.*1377C>G	NP_001293085.1:n.*1377C>G
NM_012073.3:c.*1377C>G , LRG_361t1:c.*1377C>G	NP_036205.1:n.*1377C>G
NM_012073.4:c.*1377C>G	NP_036205.1:n.*1377C>G
ENST00000280326.8:c.*1377C>G	ENSP00000280326.4:n.*1377C>G