Canonical Allele Identifier: CA395344707
Gene: CLN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28484015A>G , CM000678.2:g.28484015A>G GRCh38
NC_000016.9:g.28495336A>G , CM000678.1:g.28495336A>G GRCh37
NC_000016.8:g.28402837A>G NCBI36
NG_008654.2:g.13288T>C , LRG_689:g.13288T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333496.14:c.709T>C ENSP00000329171.9:p.Ser237Pro
ENST00000355477.10:c.637T>C ENSP00000347660.7:p.Ser213Pro
ENST00000357857.14:c.619T>C ENSP00000350523.9:p.Ser207Pro
ENST00000359984.12:c.781T>C ENSP00000353073.9:p.Ser261Pro
ENST00000360019.8:c.709T>C ENSP00000353116.3:p.Ser237Pro
ENST00000395653.9:c.322T>C ENSP00000379014.5:p.Ser108Pro
ENST00000561689.6:n.1066T>C
ENST00000564091.6:c.121T>C ENSP00000454466.2:p.Ser41Pro
ENST00000565316.6:c.781T>C ENSP00000456117.1:p.Ser261Pro
ENST00000565778.6:c.412T>C ENSP00000458015.1:p.Ser138Pro
ENST00000566083.6:n.1239T>C
ENST00000566824.6:n.761T>C
ENST00000567963.6:c.619T>C ENSP00000455387.2:p.Ser207Pro
ENST00000568076.6:n.908T>C
ENST00000568422.6:c.*18T>C ENSP00000455549.2:n.*18T>C
ENST00000568452.6:n.884T>C
ENST00000568472.6:n.657T>C
ENST00000568497.6:c.-189T>C ENSP00000456414.2:n.-189T>C
ENST00000568558.6:c.484T>C ENSP00000455603.2:p.Ser162Pro
ENST00000569430.7:c.781T>C ENSP00000454229.1:p.Ser261Pro
ENST00000628023.3:c.*77T>C ENSP00000486178.1:n.*77T>C
ENST00000635861.1:c.*305T>C ENSP00000490034.1:n.*305T>C
ENST00000635887.1:c.781T>C ENSP00000490709.1:p.Ser261Pro
ENST00000635958.1:n.892T>C
ENST00000635973.1:c.532T>C ENSP00000490363.1:p.Ser178Pro
ENST00000636017.1:c.*305T>C ENSP00000490538.1:n.*305T>C
ENST00000636078.1:n.823T>C
ENST00000636147.2:c.781T>C MANE Select ENSP00000490105.1:p.Ser261Pro
ENST00000636172.1:c.*305T>C ENSP00000490505.1:n.*305T>C
ENST00000636228.1:c.475T>C ENSP00000489627.1:p.Ser159Pro
ENST00000636351.1:n.501T>C
ENST00000636503.1:c.781T>C ENSP00000489824.1:p.Ser261Pro
ENST00000636685.1:n.288T>C
ENST00000636766.1:c.781T>C ENSP00000489841.1:p.Ser261Pro
ENST00000636839.1:n.933T>C
ENST00000636853.1:n.1696T>C
ENST00000636866.1:c.781T>C ENSP00000490880.1:p.Ser261Pro
ENST00000636907.1:n.932T>C
ENST00000636977.1:n.1849T>C
ENST00000637050.1:n.868T>C
ENST00000637100.1:c.781T>C ENSP00000490394.1:p.Ser261Pro
ENST00000637107.1:c.*305T>C ENSP00000490248.1:n.*305T>C
ENST00000637184.1:c.781T>C ENSP00000489952.1:p.Ser261Pro
ENST00000637299.1:c.*590T>C ENSP00000489823.1:n.*590T>C
ENST00000637376.1:c.781T>C ENSP00000490758.1:p.Ser261Pro
ENST00000637578.1:c.*305T>C ENSP00000490206.1:n.*305T>C
ENST00000637699.1:c.564T>C ENSP00000490049.1:n.564T>C
ENST00000637745.1:c.120T>C
ENST00000637871.1:c.*305T>C ENSP00000490670.1:n.*305T>C
ENST00000333496.13:c.709T>C ENSP00000329171.9:p.Ser237Pro
ENST00000355477.9:c.*18T>C ENSP00000347660.6:n.*18T>C
ENST00000357806.11:c.484T>C ENSP00000350457.7:p.Ser162Pro
ENST00000357857.13:c.619T>C ENSP00000350523.9:p.Ser207Pro
ENST00000359984.11:c.475T>C ENSP00000353073.8:p.Ser159Pro
ENST00000360019.6:c.781T>C ENSP00000353116.2:p.Ser261Pro
ENST00000395653.8:c.481T>C ENSP00000379014.4:p.Ser161Pro
ENST00000561689.5:n.622T>C
ENST00000563874.5:n.2135T>C
ENST00000564574.5:n.829T>C
ENST00000565047.1:n.375T>C
ENST00000565140.5:c.564T>C ENSP00000455342.1:n.564T>C
ENST00000565316.5:c.781T>C ENSP00000456117.1:p.Ser261Pro
ENST00000565778.5:c.412T>C ENSP00000458015.1:p.Ser138Pro
ENST00000566057.5:c.395T>C ENSP00000456693.1:n.395T>C
ENST00000566083.5:n.1012T>C
ENST00000566824.5:n.830T>C
ENST00000567495.5:c.*18T>C ENSP00000456013.1:n.*18T>C
ENST00000567963.5:c.781T>C ENSP00000455387.1:p.Ser261Pro
ENST00000568076.5:n.564T>C
ENST00000568224.4:c.547T>C ENSP00000454253.1:p.Ser183Pro
ENST00000568422.5:c.*18T>C ENSP00000455549.1:n.*18T>C
ENST00000568452.5:n.781T>C
ENST00000568472.5:n.261T>C
ENST00000568497.5:c.*77T>C ENSP00000456414.1:n.*77T>C
ENST00000568558.5:c.322T>C ENSP00000455603.1:p.Ser108Pro
ENST00000569030.5:c.461-1343T>C ENSP00000454680.1:n.461-1343T>C
ENST00000569430.5:c.781T>C ENSP00000454229.1:p.Ser261Pro
ENST00000628023.2:c.*77T>C ENSP00000486178.1:n.*77T>C
ENST00000631023.2:c.781T>C ENSP00000486616.1:p.Ser261Pro
NM_000086.2:c.781T>C , LRG_689t1:c.781T>C NP_000077.1:p.Ser261Pro
NM_001042432.1:c.781T>C , LRG_689t2:c.781T>C NP_001035897.1:p.Ser261Pro
NM_001286104.1:c.709T>C NP_001273033.1:p.Ser237Pro
NM_001286105.1:c.481T>C NP_001273034.1:p.Ser161Pro
NM_001286109.1:c.547T>C NP_001273038.1:p.Ser183Pro
NM_001286110.1:c.619T>C NP_001273039.1:p.Ser207Pro
NM_001042432.2:c.781T>C MANE Select NP_001035897.1:p.Ser261Pro
NM_001286104.2:c.709T>C NP_001273033.1:p.Ser237Pro
NM_001286105.2:c.481T>C NP_001273034.1:p.Ser161Pro
NM_001286109.2:c.547T>C NP_001273038.1:p.Ser183Pro
NM_001286110.2:c.619T>C NP_001273039.1:p.Ser207Pro