Canonical Allele Identifier: CA443258164

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256125A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256013A>C , CM000667.2:g.10256013A>C	GRCh38
NC_000005.9:g.10256125A>C , CM000667.1:g.10256125A>C	GRCh37
NC_000005.8:g.10309125A>C	NCBI36
NG_012160.1:g.10844A>C , LRG_361:g.10844A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.390A>C MANE Select	ENSP00000280326.4:p.Pro130=
ENST00000280326.8:c.390A>C	ENSP00000280326.4:p.Pro130=
ENST00000423695.6:n.128-2098A>C
ENST00000503026.5:c.327A>C	ENSP00000423318.1:p.Pro109=
ENST00000503454.5:c.279A>C
ENST00000506600.1:c.111A>C	ENSP00000423052.1:p.Pro37=
ENST00000511700.1:c.305A>C	ENSP00000423087.1:n.305A>C
ENST00000512975.5:c.106-2098A>C	ENSP00000425751.1:n.106-2098A>C
ENST00000515390.5:c.225A>C	ENSP00000426923.1:p.Pro75=
ENST00000515676.5:c.276A>C	ENSP00000427297.1:p.Pro92=
ENST00000625723.1:c.106-2098A>C	ENSP00000487128.1:n.106-2098A>C
NM_001306153.1:c.327A>C	NP_001293082.1:p.Pro109=
NM_001306154.1:c.225A>C	NP_001293083.1:p.Pro75=
NM_001306155.1:c.111A>C	NP_001293084.1:p.Pro37=
NM_001306156.1:c.276A>C	NP_001293085.1:p.Pro92=
NM_012073.3:c.390A>C , LRG_361t1:c.390A>C	NP_036205.1:p.Pro130=
NM_012073.4:c.390A>C	NP_036205.1:p.Pro130=
NM_012073.5:c.390A>C MANE Select	NP_036205.1:p.Pro130=
NM_001306154.2:c.225A>C	NP_001293083.1:p.Pro75=
NM_001306155.2:c.111A>C	NP_001293084.1:p.Pro37=
NM_001306156.2:c.276A>C	NP_001293085.1:p.Pro92=