Canonical Allele Identifier: CA359181229

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256130G>C (hg19) ; chr5:g.10256018G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256018G>C , CM000667.2:g.10256018G>C	GRCh38
NC_000005.9:g.10256130G>C , CM000667.1:g.10256130G>C	GRCh37
NC_000005.8:g.10309130G>C	NCBI36
NG_012160.1:g.10849G>C , LRG_361:g.10849G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.395G>C MANE Select	ENSP00000280326.4:p.Arg132Thr
ENST00000280326.8:c.395G>C	ENSP00000280326.4:p.Arg132Thr
ENST00000423695.6:n.128-2093G>C
ENST00000503026.5:c.332G>C	ENSP00000423318.1:p.Arg111Thr
ENST00000503454.5:c.284G>C
ENST00000506600.1:c.116G>C	ENSP00000423052.1:p.Arg39Thr
ENST00000511700.1:c.310G>C	ENSP00000423087.1:n.310G>C
ENST00000512975.5:c.106-2093G>C	ENSP00000425751.1:n.106-2093G>C
ENST00000515390.5:c.230G>C	ENSP00000426923.1:p.Arg77Thr
ENST00000515676.5:c.281G>C	ENSP00000427297.1:p.Arg94Thr
ENST00000625723.1:c.106-2093G>C	ENSP00000487128.1:n.106-2093G>C
NM_001306153.1:c.332G>C	NP_001293082.1:p.Arg111Thr
NM_001306154.1:c.230G>C	NP_001293083.1:p.Arg77Thr
NM_001306155.1:c.116G>C	NP_001293084.1:p.Arg39Thr
NM_001306156.1:c.281G>C	NP_001293085.1:p.Arg94Thr
NM_012073.3:c.395G>C , LRG_361t1:c.395G>C	NP_036205.1:p.Arg132Thr
NM_012073.4:c.395G>C	NP_036205.1:p.Arg132Thr
NM_012073.5:c.395G>C MANE Select	NP_036205.1:p.Arg132Thr
NM_001306154.2:c.230G>C	NP_001293083.1:p.Arg77Thr
NM_001306155.2:c.116G>C	NP_001293084.1:p.Arg39Thr
NM_001306156.2:c.281G>C	NP_001293085.1:p.Arg94Thr