Canonical Allele Identifier: CA359181056

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256087G>A (hg19) ; chr5:g.10255975G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255975G>A , CM000667.2:g.10255975G>A	GRCh38
NC_000005.9:g.10256087G>A , CM000667.1:g.10256087G>A	GRCh37
NC_000005.8:g.10309087G>A	NCBI36
NG_012160.1:g.10806G>A , LRG_361:g.10806G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.352G>A MANE Select	ENSP00000280326.4:p.Glu118Lys
ENST00000280326.8:c.352G>A	ENSP00000280326.4:p.Glu118Lys
ENST00000423695.6:n.128-2136G>A
ENST00000503026.5:c.289G>A	ENSP00000423318.1:p.Glu97Lys
ENST00000503454.5:c.241G>A
ENST00000506600.1:c.73G>A	ENSP00000423052.1:p.Glu25Lys
ENST00000511700.1:c.267G>A	ENSP00000423087.1:p.Ter89=
ENST00000512975.5:c.106-2136G>A	ENSP00000425751.1:n.106-2136G>A
ENST00000515390.5:c.187G>A	ENSP00000426923.1:p.Glu63Lys
ENST00000515676.5:c.238G>A	ENSP00000427297.1:p.Glu80Lys
ENST00000625723.1:c.106-2136G>A	ENSP00000487128.1:n.106-2136G>A
NM_001306153.1:c.289G>A	NP_001293082.1:p.Glu97Lys
NM_001306154.1:c.187G>A	NP_001293083.1:p.Glu63Lys
NM_001306155.1:c.73G>A	NP_001293084.1:p.Glu25Lys
NM_001306156.1:c.238G>A	NP_001293085.1:p.Glu80Lys
NM_012073.3:c.352G>A , LRG_361t1:c.352G>A	NP_036205.1:p.Glu118Lys
NM_012073.4:c.352G>A	NP_036205.1:p.Glu118Lys
NM_012073.5:c.352G>A MANE Select	NP_036205.1:p.Glu118Lys
NM_001306154.2:c.187G>A	NP_001293083.1:p.Glu63Lys
NM_001306155.2:c.73G>A	NP_001293084.1:p.Glu25Lys
NM_001306156.2:c.238G>A	NP_001293085.1:p.Glu80Lys