Canonical Allele Identifier: CA3198084
Gene: CCT5 HGNC NCBI

Linked Data

dbSNP Id: rs752539971

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10256083A>G , CM000667.2:g.10256083A>G GRCh38
NC_000005.9:g.10256195A>G , CM000667.1:g.10256195A>G GRCh37
NC_000005.8:g.10309195A>G NCBI36
NG_012160.1:g.10914A>G , LRG_361:g.10914A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000280326.9:c.460A>G MANE Select ENSP00000280326.4:p.Ser154Gly
ENST00000280326.8:c.460A>G ENSP00000280326.4:p.Ser154Gly
ENST00000423695.6:n.128-2028A>G
ENST00000503026.5:c.397A>G ENSP00000423318.1:p.Ser133Gly
ENST00000503454.5:c.349A>G
ENST00000506600.1:c.181A>G ENSP00000423052.1:p.Ser61Gly
ENST00000511700.1:c.375A>G ENSP00000423087.1:n.375A>G
ENST00000512975.5:c.106-2028A>G ENSP00000425751.1:n.106-2028A>G
ENST00000515390.5:c.295A>G ENSP00000426923.1:p.Ser99Gly
ENST00000515676.5:c.346A>G ENSP00000427297.1:p.Ser116Gly
ENST00000625723.1:c.106-2028A>G ENSP00000487128.1:n.106-2028A>G
NM_001306153.1:c.397A>G NP_001293082.1:p.Ser133Gly
NM_001306154.1:c.295A>G NP_001293083.1:p.Ser99Gly
NM_001306155.1:c.181A>G NP_001293084.1:p.Ser61Gly
NM_001306156.1:c.346A>G NP_001293085.1:p.Ser116Gly
NM_012073.3:c.460A>G , LRG_361t1:c.460A>G NP_036205.1:p.Ser154Gly
NM_012073.4:c.460A>G NP_036205.1:p.Ser154Gly
NM_012073.5:c.460A>G MANE Select NP_036205.1:p.Ser154Gly
NM_001306154.2:c.295A>G NP_001293083.1:p.Ser99Gly
NM_001306155.2:c.181A>G NP_001293084.1:p.Ser61Gly
NM_001306156.2:c.346A>G NP_001293085.1:p.Ser116Gly