Canonical Allele Identifier: CA1526932812
Gene: CCT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10255983G= , CM000667.2:g.10255983G= GRCh38
NC_000005.9:g.10256095G= , CM000667.1:g.10256095G= GRCh37
NC_000005.8:g.10309095G= NCBI36
NG_012160.1:g.10814G= , LRG_361:g.10814G=

Transcript Alleles

HGVS Amino-acid change
ENST00000280326.9:c.360G= MANE Select ENSP00000280326.4:p.Ala120=
ENST00000280326.8:c.360G= ENSP00000280326.4:p.Ala120=
ENST00000423695.6:n.128-2128G=
ENST00000503026.5:c.297G= ENSP00000423318.1:p.Ala99=
ENST00000503454.5:c.249G=
ENST00000506600.1:c.81G= ENSP00000423052.1:p.Ala27=
ENST00000511700.1:c.275G= ENSP00000423087.1:n.275G=
ENST00000512975.5:c.106-2128G= ENSP00000425751.1:n.106-2128G=
ENST00000515390.5:c.195G= ENSP00000426923.1:p.Ala65=
ENST00000515676.5:c.246G= ENSP00000427297.1:p.Ala82=
ENST00000625723.1:c.106-2128G= ENSP00000487128.1:n.106-2128G=
NM_001306153.1:c.297G= NP_001293082.1:p.Ala99=
NM_001306154.1:c.195G= NP_001293083.1:p.Ala65=
NM_001306155.1:c.81G= NP_001293084.1:p.Ala27=
NM_001306156.1:c.246G= NP_001293085.1:p.Ala82=
NM_012073.3:c.360G= , LRG_361t1:c.360G= NP_036205.1:p.Ala120=
NM_012073.4:c.360G= NP_036205.1:p.Ala120=
NM_012073.5:c.360G= MANE Select NP_036205.1:p.Ala120=
NM_001306154.2:c.195G= NP_001293083.1:p.Ala65=
NM_001306155.2:c.81G= NP_001293084.1:p.Ala27=
NM_001306156.2:c.246G= NP_001293085.1:p.Ala82=