Canonical Allele Identifier: CA3198046

Gene: CCT5

Linked Data

• dbSNP Id: rs766153615
• ExAC: 5:10256027 G / C
• gnomAD v2: 5-10256027-G-C
• MyVariant Identifiers: chr5:g.10256027G>C (hg19) ; chr5:g.10255915G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255915G>C , CM000667.2:g.10255915G>C	GRCh38
NC_000005.9:g.10256027G>C , CM000667.1:g.10256027G>C	GRCh37
NC_000005.8:g.10309027G>C	NCBI36
NG_012160.1:g.10746G>C , LRG_361:g.10746G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.332-40G>C MANE Select	ENSP00000280326.4:n.332-40G>C
ENST00000280326.8:c.332-40G>C	ENSP00000280326.4:n.332-40G>C
ENST00000423695.6:n.128-2196G>C
ENST00000503026.5:c.269-40G>C	ENSP00000423318.1:n.269-40G>C
ENST00000503454.5:c.221-40G>C
ENST00000506600.1:c.53-40G>C	ENSP00000423052.1:n.53-40G>C
ENST00000511700.1:c.247-40G>C	ENSP00000423087.1:n.247-40G>C
ENST00000512975.5:c.106-2196G>C	ENSP00000425751.1:n.106-2196G>C
ENST00000515390.5:c.167-40G>C	ENSP00000426923.1:n.167-40G>C
ENST00000515676.5:c.218-40G>C	ENSP00000427297.1:n.218-40G>C
ENST00000625723.1:c.106-2196G>C	ENSP00000487128.1:n.106-2196G>C
NM_001306153.1:c.269-40G>C	NP_001293082.1:n.269-40G>C
NM_001306154.1:c.167-40G>C	NP_001293083.1:n.167-40G>C
NM_001306155.1:c.53-40G>C	NP_001293084.1:n.53-40G>C
NM_001306156.1:c.218-40G>C	NP_001293085.1:n.218-40G>C
NM_012073.3:c.332-40G>C , LRG_361t1:c.332-40G>C	NP_036205.1:n.332-40G>C
NM_012073.4:c.332-40G>C	NP_036205.1:n.332-40G>C
NM_012073.5:c.332-40G>C MANE Select	NP_036205.1:n.332-40G>C
NM_001306154.2:c.167-40G>C	NP_001293083.1:n.167-40G>C
NM_001306155.2:c.53-40G>C	NP_001293084.1:n.53-40G>C
NM_001306156.2:c.218-40G>C	NP_001293085.1:n.218-40G>C