Canonical Allele Identifier: CA2215697773
Gene: CLN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28482112_28482113delinsAG , CM000678.2:g.28482112_28482113delinsAG GRCh38
NC_000016.9:g.28493433_28493434delinsAG , CM000678.1:g.28493433_28493434delinsAG GRCh37
NC_000016.8:g.28400934_28400935delinsAG NCBI36
NG_008654.2:g.15190_15191delinsCT , LRG_689:g.15190_15191delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000333496.14:c.976_977delinsCT ENSP00000329171.9:p.Leu326=
ENST00000355477.10:c.904_905delinsCT ENSP00000347660.7:p.Leu302=
ENST00000357857.14:c.886_887delinsCT ENSP00000350523.9:p.Leu296=
ENST00000359984.12:c.1048_1049delinsCT ENSP00000353073.9:p.Leu350=
ENST00000360019.8:c.976_977delinsCT ENSP00000353116.3:p.Leu326=
ENST00000395653.9:c.589_590delinsCT ENSP00000379014.5:p.Leu197=
ENST00000561689.6:n.1461_1462delinsCT
ENST00000564091.6:c.388_389delinsCT ENSP00000454466.2:p.Leu130=
ENST00000565316.6:c.997_998delinsCT ENSP00000456117.1:p.Leu333=
ENST00000566824.6:n.1108_1109delinsCT
ENST00000567963.6:c.886_887delinsCT ENSP00000455387.2:p.Leu296=
ENST00000568076.6:n.1477_1478delinsCT
ENST00000568422.6:c.*285_*286delinsCT ENSP00000455549.2:n.*285_*286delinsCT
ENST00000568452.6:n.1279_1280delinsCT
ENST00000568497.6:c.79_80delinsCT ENSP00000456414.2:p.Leu27=
ENST00000569430.7:c.1048_1049delinsCT ENSP00000454229.1:p.Leu350=
ENST00000628023.3:c.*344_*345delinsCT ENSP00000486178.1:n.*344_*345delinsCT
ENST00000635861.1:c.*700_*701delinsCT ENSP00000490034.1:n.*700_*701delinsCT
ENST00000635887.1:c.1048_1049delinsCT ENSP00000490709.1:p.Leu350=
ENST00000635958.1:n.1333_1334delinsCT
ENST00000635973.1:c.799_800delinsCT ENSP00000490363.1:p.Leu267=
ENST00000636017.1:c.*572_*573delinsCT ENSP00000490538.1:n.*572_*573delinsCT
ENST00000636078.1:n.1170_1171delinsCT
ENST00000636147.2:c.1048_1049delinsCT MANE Select ENSP00000490105.1:p.Leu350=
ENST00000636172.1:c.*572_*573delinsCT ENSP00000490505.1:n.*572_*573delinsCT
ENST00000636228.1:c.742_743delinsCT ENSP00000489627.1:p.Leu248=
ENST00000636351.1:n.942_943delinsCT
ENST00000636503.1:c.1048_1049delinsCT ENSP00000489824.1:p.Leu350=
ENST00000636685.1:n.729_730delinsCT
ENST00000636766.1:c.1048_1049delinsCT ENSP00000489841.1:p.Leu350=
ENST00000636839.1:n.1422_1423delinsCT
ENST00000636853.1:n.1963_1964delinsCT
ENST00000636866.1:c.1048_1049delinsCT ENSP00000490880.1:p.Leu350=
ENST00000636907.1:n.1199_1200delinsCT
ENST00000636977.1:n.2418_2419delinsCT
ENST00000637050.1:n.1437_1438delinsCT
ENST00000637100.1:c.997_998delinsCT ENSP00000490394.1:p.Leu333=
ENST00000637107.1:c.*572_*573delinsCT ENSP00000490248.1:n.*572_*573delinsCT
ENST00000637184.1:c.1048_1049delinsCT ENSP00000489952.1:p.Leu350=
ENST00000637299.1:c.*857_*858delinsCT ENSP00000489823.1:n.*857_*858delinsCT
ENST00000637376.1:c.1048_1049delinsCT ENSP00000490758.1:p.Leu350=
ENST00000637378.1:c.220_221delinsCT ENSP00000490831.1:p.Leu74=
ENST00000637578.1:c.*572_*573delinsCT ENSP00000490206.1:n.*572_*573delinsCT
ENST00000637699.1:c.959_960delinsCT ENSP00000490049.1:n.959_960delinsCT
ENST00000637745.1:c.387_388delinsCT
ENST00000637871.1:c.*746_*747delinsCT ENSP00000490670.1:n.*746_*747delinsCT
ENST00000638036.1:c.210_211delinsCT
ENST00000333496.13:c.976_977delinsCT ENSP00000329171.9:p.Leu326=
ENST00000355477.9:c.*285_*286delinsCT ENSP00000347660.6:n.*285_*286delinsCT
ENST00000357806.11:c.751_752delinsCT ENSP00000350457.7:p.Leu251=
ENST00000357857.13:c.886_887delinsCT ENSP00000350523.9:p.Leu296=
ENST00000359984.11:c.742_743delinsCT ENSP00000353073.8:p.Leu248=
ENST00000360019.6:c.1048_1049delinsCT ENSP00000353116.2:p.Leu350=
ENST00000395653.8:c.748_749delinsCT ENSP00000379014.4:p.Leu250=
ENST00000561689.5:n.1017_1018delinsCT
ENST00000563874.5:n.2576_2577delinsCT
ENST00000564091.5:c.137_138delinsCT
ENST00000565140.5:c.831_832delinsCT ENSP00000455342.1:n.831_832delinsCT
ENST00000565316.5:c.997_998delinsCT ENSP00000456117.1:p.Leu333=
ENST00000565354.5:n.361_362delinsCT
ENST00000566057.5:c.662_663delinsCT ENSP00000456693.1:n.662_663delinsCT
ENST00000567963.5:c.906+364_906+365delinsCT ENSP00000455387.1:n.906+364_906+365delinsCT
ENST00000568076.5:n.959_960delinsCT
ENST00000568224.4:c.814_815delinsCT ENSP00000454253.1:p.Leu272=
ENST00000568422.5:c.*285_*286delinsCT ENSP00000455549.1:n.*285_*286delinsCT
ENST00000568452.5:n.1176_1177delinsCT
ENST00000569030.5:c.718_719delinsCT ENSP00000454680.1:p.Leu240=
ENST00000569430.5:c.1048_1049delinsCT ENSP00000454229.1:p.Leu350=
ENST00000628023.2:c.*344_*345delinsCT ENSP00000486178.1:n.*344_*345delinsCT
ENST00000631023.2:c.906+364_906+365delinsCT ENSP00000486616.1:n.906+364_906+365delinsCT
NM_000086.2:c.1048_1049delinsCT , LRG_689t1:c.1048_1049delinsCT NP_000077.1:p.Leu350=
NM_001042432.1:c.1048_1049delinsCT , LRG_689t2:c.1048_1049delinsCT NP_001035897.1:p.Leu350=
NM_001286104.1:c.976_977delinsCT NP_001273033.1:p.Leu326=
NM_001286105.1:c.748_749delinsCT NP_001273034.1:p.Leu250=
NM_001286109.1:c.814_815delinsCT NP_001273038.1:p.Leu272=
NM_001286110.1:c.886_887delinsCT NP_001273039.1:p.Leu296=
NM_001042432.2:c.1048_1049delinsCT MANE Select NP_001035897.1:p.Leu350=
NM_001286104.2:c.976_977delinsCT NP_001273033.1:p.Leu326=
NM_001286105.2:c.748_749delinsCT NP_001273034.1:p.Leu250=
NM_001286109.2:c.814_815delinsCT NP_001273038.1:p.Leu272=
NM_001286110.2:c.886_887delinsCT NP_001273039.1:p.Leu296=