Canonical Allele Identifier: CA359181645

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256265T>C (hg19) ; chr5:g.10256153T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256153T>C , CM000667.2:g.10256153T>C	GRCh38
NC_000005.9:g.10256265T>C , CM000667.1:g.10256265T>C	GRCh37
NC_000005.8:g.10309265T>C	NCBI36
NG_012160.1:g.10984T>C , LRG_361:g.10984T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.530T>C MANE Select	ENSP00000280326.4:p.Val177Ala
ENST00000280326.8:c.530T>C	ENSP00000280326.4:p.Val177Ala
ENST00000423695.6:n.128-1958T>C
ENST00000503026.5:c.467T>C	ENSP00000423318.1:p.Val156Ala
ENST00000503454.5:c.419T>C
ENST00000506600.1:c.251T>C	ENSP00000423052.1:p.Val84Ala
ENST00000511700.1:c.445T>C	ENSP00000423087.1:n.445T>C
ENST00000512975.5:c.106-1958T>C	ENSP00000425751.1:n.106-1958T>C
ENST00000515390.5:c.365T>C	ENSP00000426923.1:p.Val122Ala
ENST00000515676.5:c.416T>C	ENSP00000427297.1:p.Val139Ala
ENST00000625723.1:c.106-1958T>C	ENSP00000487128.1:n.106-1958T>C
NM_001306153.1:c.467T>C	NP_001293082.1:p.Val156Ala
NM_001306154.1:c.365T>C	NP_001293083.1:p.Val122Ala
NM_001306155.1:c.251T>C	NP_001293084.1:p.Val84Ala
NM_001306156.1:c.416T>C	NP_001293085.1:p.Val139Ala
NM_012073.3:c.530T>C , LRG_361t1:c.530T>C	NP_036205.1:p.Val177Ala
NM_012073.4:c.530T>C	NP_036205.1:p.Val177Ala
NM_012073.5:c.530T>C MANE Select	NP_036205.1:p.Val177Ala
NM_001306154.2:c.365T>C	NP_001293083.1:p.Val122Ala
NM_001306155.2:c.251T>C	NP_001293084.1:p.Val84Ala
NM_001306156.2:c.416T>C	NP_001293085.1:p.Val139Ala