Canonical Allele Identifier: CA359181402

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256190G>C (hg19) ; chr5:g.10256078G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256078G>C , CM000667.2:g.10256078G>C	GRCh38
NC_000005.9:g.10256190G>C , CM000667.1:g.10256190G>C	GRCh37
NC_000005.8:g.10309190G>C	NCBI36
NG_012160.1:g.10909G>C , LRG_361:g.10909G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.455G>C MANE Select	ENSP00000280326.4:p.Ser152Thr
ENST00000280326.8:c.455G>C	ENSP00000280326.4:p.Ser152Thr
ENST00000423695.6:n.128-2033G>C
ENST00000503026.5:c.392G>C	ENSP00000423318.1:p.Ser131Thr
ENST00000503454.5:c.344G>C
ENST00000506600.1:c.176G>C	ENSP00000423052.1:p.Ser59Thr
ENST00000511700.1:c.370G>C	ENSP00000423087.1:n.370G>C
ENST00000512975.5:c.106-2033G>C	ENSP00000425751.1:n.106-2033G>C
ENST00000515390.5:c.290G>C	ENSP00000426923.1:p.Ser97Thr
ENST00000515676.5:c.341G>C	ENSP00000427297.1:p.Ser114Thr
ENST00000625723.1:c.106-2033G>C	ENSP00000487128.1:n.106-2033G>C
NM_001306153.1:c.392G>C	NP_001293082.1:p.Ser131Thr
NM_001306154.1:c.290G>C	NP_001293083.1:p.Ser97Thr
NM_001306155.1:c.176G>C	NP_001293084.1:p.Ser59Thr
NM_001306156.1:c.341G>C	NP_001293085.1:p.Ser114Thr
NM_012073.3:c.455G>C , LRG_361t1:c.455G>C	NP_036205.1:p.Ser152Thr
NM_012073.4:c.455G>C	NP_036205.1:p.Ser152Thr
NM_012073.5:c.455G>C MANE Select	NP_036205.1:p.Ser152Thr
NM_001306154.2:c.290G>C	NP_001293083.1:p.Ser97Thr
NM_001306155.2:c.176G>C	NP_001293084.1:p.Ser59Thr
NM_001306156.2:c.341G>C	NP_001293085.1:p.Ser114Thr