Canonical Allele Identifier: CA395344921
Gene: CLN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28484097A>C , CM000678.2:g.28484097A>C GRCh38
NC_000016.9:g.28495418A>C , CM000678.1:g.28495418A>C GRCh37
NC_000016.8:g.28402919A>C NCBI36
NG_008654.2:g.13206T>G , LRG_689:g.13206T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333496.14:c.627T>G ENSP00000329171.9:p.Ser209=
ENST00000355477.10:c.555T>G ENSP00000347660.7:p.Ser185=
ENST00000357857.14:c.537T>G ENSP00000350523.9:p.Ser179=
ENST00000359984.12:c.699T>G ENSP00000353073.9:p.Ser233=
ENST00000360019.8:c.627T>G ENSP00000353116.3:p.Ser209=
ENST00000395653.9:c.240T>G ENSP00000379014.5:p.Ser80=
ENST00000561689.6:n.984T>G
ENST00000564091.6:c.39T>G ENSP00000454466.2:p.Ser13=
ENST00000565316.6:c.699T>G ENSP00000456117.1:p.Ser233=
ENST00000565778.6:c.330T>G ENSP00000458015.1:p.Ser110=
ENST00000566083.6:n.1157T>G
ENST00000566824.6:n.679T>G
ENST00000567495.6:c.*158T>G ENSP00000456013.2:n.*158T>G
ENST00000567963.6:c.537T>G ENSP00000455387.2:p.Ser179=
ENST00000568076.6:n.826T>G
ENST00000568422.6:c.482T>G ENSP00000455549.2:p.Leu161Arg
ENST00000568452.6:n.802T>G
ENST00000568472.6:n.575T>G
ENST00000568497.6:c.-271T>G ENSP00000456414.2:n.-271T>G
ENST00000568558.6:c.402T>G ENSP00000455603.2:p.Ser134=
ENST00000569430.7:c.699T>G ENSP00000454229.1:p.Ser233=
ENST00000628023.3:c.244T>G ENSP00000486178.1:p.Ser82Ala
ENST00000635861.1:c.*223T>G ENSP00000490034.1:n.*223T>G
ENST00000635887.1:c.699T>G ENSP00000490709.1:p.Ser233=
ENST00000635958.1:n.810T>G
ENST00000635973.1:c.450T>G ENSP00000490363.1:p.Ser150=
ENST00000636017.1:c.*223T>G ENSP00000490538.1:n.*223T>G
ENST00000636078.1:n.741T>G
ENST00000636147.2:c.699T>G MANE Select ENSP00000490105.1:p.Ser233=
ENST00000636172.1:c.*223T>G ENSP00000490505.1:n.*223T>G
ENST00000636228.1:c.393T>G ENSP00000489627.1:p.Ser131=
ENST00000636351.1:n.419T>G
ENST00000636503.1:c.699T>G ENSP00000489824.1:p.Ser233=
ENST00000636685.1:n.206T>G
ENST00000636766.1:c.699T>G ENSP00000489841.1:p.Ser233=
ENST00000636839.1:n.851T>G
ENST00000636853.1:n.1614T>G
ENST00000636866.1:c.699T>G ENSP00000490880.1:p.Ser233=
ENST00000636907.1:n.850T>G
ENST00000636977.1:n.1767T>G
ENST00000637050.1:n.786T>G
ENST00000637100.1:c.699T>G ENSP00000490394.1:p.Ser233=
ENST00000637107.1:c.*223T>G ENSP00000490248.1:n.*223T>G
ENST00000637184.1:c.699T>G ENSP00000489952.1:p.Ser233=
ENST00000637299.1:c.*508T>G ENSP00000489823.1:n.*508T>G
ENST00000637376.1:c.699T>G ENSP00000490758.1:p.Ser233=
ENST00000637578.1:c.*223T>G ENSP00000490206.1:n.*223T>G
ENST00000637699.1:c.482T>G ENSP00000490049.1:p.Leu161Arg
ENST00000637745.1:c.38T>G
ENST00000637871.1:c.*223T>G ENSP00000490670.1:n.*223T>G
ENST00000333496.13:c.627T>G ENSP00000329171.9:p.Ser209=
ENST00000355477.9:c.482T>G ENSP00000347660.6:p.Leu161Arg
ENST00000357806.11:c.402T>G ENSP00000350457.7:p.Ser134=
ENST00000357857.13:c.537T>G ENSP00000350523.9:p.Ser179=
ENST00000359984.11:c.393T>G ENSP00000353073.8:p.Ser131=
ENST00000360019.6:c.699T>G ENSP00000353116.2:p.Ser233=
ENST00000395653.8:c.399T>G ENSP00000379014.4:p.Ser133=
ENST00000561689.5:n.540T>G
ENST00000563874.5:n.2053T>G
ENST00000564574.5:n.747T>G
ENST00000565047.1:n.293T>G
ENST00000565140.5:c.482T>G ENSP00000455342.1:p.Leu161Arg
ENST00000565316.5:c.699T>G ENSP00000456117.1:p.Ser233=
ENST00000565688.5:c.450T>G ENSP00000456122.1:p.Ser150=
ENST00000565778.5:c.330T>G ENSP00000458015.1:p.Ser110=
ENST00000566057.5:c.313T>G ENSP00000456693.1:p.Ser105Ala
ENST00000566083.5:n.930T>G
ENST00000566824.5:n.748T>G
ENST00000567495.5:c.482T>G ENSP00000456013.1:p.Leu161Arg
ENST00000567963.5:c.699T>G ENSP00000455387.1:p.Ser233=
ENST00000568076.5:n.482T>G
ENST00000568224.4:c.465T>G ENSP00000454253.1:p.Ser155=
ENST00000568422.5:c.335T>G ENSP00000455549.1:p.Leu112Arg
ENST00000568452.5:n.699T>G
ENST00000568472.5:n.179T>G
ENST00000568497.5:c.244T>G ENSP00000456414.1:p.Ser82Ala
ENST00000568558.5:c.240T>G ENSP00000455603.1:p.Ser80=
ENST00000569030.5:c.461-1425T>G ENSP00000454680.1:n.461-1425T>G
ENST00000569430.5:c.699T>G ENSP00000454229.1:p.Ser233=
ENST00000628023.2:c.244T>G ENSP00000486178.1:p.Ser82Ala
ENST00000631023.2:c.699T>G ENSP00000486616.1:p.Ser233=
NM_000086.2:c.699T>G , LRG_689t1:c.699T>G NP_000077.1:p.Ser233=
NM_001042432.1:c.699T>G , LRG_689t2:c.699T>G NP_001035897.1:p.Ser233=
NM_001286104.1:c.627T>G NP_001273033.1:p.Ser209=
NM_001286105.1:c.399T>G NP_001273034.1:p.Ser133=
NM_001286109.1:c.465T>G NP_001273038.1:p.Ser155=
NM_001286110.1:c.537T>G NP_001273039.1:p.Ser179=
NM_001042432.2:c.699T>G MANE Select NP_001035897.1:p.Ser233=
NM_001286104.2:c.627T>G NP_001273033.1:p.Ser209=
NM_001286105.2:c.399T>G NP_001273034.1:p.Ser133=
NM_001286109.2:c.465T>G NP_001273038.1:p.Ser155=
NM_001286110.2:c.537T>G NP_001273039.1:p.Ser179=