Canonical Allele Identifier: CA443258418

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256194T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256082T>C , CM000667.2:g.10256082T>C	GRCh38
NC_000005.9:g.10256194T>C , CM000667.1:g.10256194T>C	GRCh37
NC_000005.8:g.10309194T>C	NCBI36
NG_012160.1:g.10913T>C , LRG_361:g.10913T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.459T>C MANE Select	ENSP00000280326.4:p.Asp153=
ENST00000280326.8:c.459T>C	ENSP00000280326.4:p.Asp153=
ENST00000423695.6:n.128-2029T>C
ENST00000503026.5:c.396T>C	ENSP00000423318.1:p.Asp132=
ENST00000503454.5:c.348T>C
ENST00000506600.1:c.180T>C	ENSP00000423052.1:p.Asp60=
ENST00000511700.1:c.374T>C	ENSP00000423087.1:n.374T>C
ENST00000512975.5:c.106-2029T>C	ENSP00000425751.1:n.106-2029T>C
ENST00000515390.5:c.294T>C	ENSP00000426923.1:p.Asp98=
ENST00000515676.5:c.345T>C	ENSP00000427297.1:p.Asp115=
ENST00000625723.1:c.106-2029T>C	ENSP00000487128.1:n.106-2029T>C
NM_001306153.1:c.396T>C	NP_001293082.1:p.Asp132=
NM_001306154.1:c.294T>C	NP_001293083.1:p.Asp98=
NM_001306155.1:c.180T>C	NP_001293084.1:p.Asp60=
NM_001306156.1:c.345T>C	NP_001293085.1:p.Asp115=
NM_012073.3:c.459T>C , LRG_361t1:c.459T>C	NP_036205.1:p.Asp153=
NM_012073.4:c.459T>C	NP_036205.1:p.Asp153=
NM_012073.5:c.459T>C MANE Select	NP_036205.1:p.Asp153=
NM_001306154.2:c.294T>C	NP_001293083.1:p.Asp98=
NM_001306155.2:c.180T>C	NP_001293084.1:p.Asp60=
NM_001306156.2:c.345T>C	NP_001293085.1:p.Asp115=