Canonical Allele Identifier: CA395344701
Gene: CLN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28484011T>G , CM000678.2:g.28484011T>G GRCh38
NC_000016.9:g.28495332T>G , CM000678.1:g.28495332T>G GRCh37
NC_000016.8:g.28402833T>G NCBI36
NG_008654.2:g.13292A>C , LRG_689:g.13292A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333496.14:c.713A>C ENSP00000329171.9:p.Lys238Thr
ENST00000355477.10:c.641A>C ENSP00000347660.7:p.Lys214Thr
ENST00000357857.14:c.623A>C ENSP00000350523.9:p.Lys208Thr
ENST00000359984.12:c.785A>C ENSP00000353073.9:p.Lys262Thr
ENST00000360019.8:c.713A>C ENSP00000353116.3:p.Lys238Thr
ENST00000395653.9:c.326A>C ENSP00000379014.5:p.Lys109Thr
ENST00000561689.6:n.1070A>C
ENST00000564091.6:c.125A>C ENSP00000454466.2:p.Lys42Thr
ENST00000565316.6:c.785A>C ENSP00000456117.1:p.Lys262Thr
ENST00000565778.6:c.416A>C ENSP00000458015.1:p.Lys139Thr
ENST00000566083.6:n.1243A>C
ENST00000566824.6:n.765A>C
ENST00000567963.6:c.623A>C ENSP00000455387.2:p.Lys208Thr
ENST00000568076.6:n.912A>C
ENST00000568422.6:c.*22A>C ENSP00000455549.2:n.*22A>C
ENST00000568452.6:n.888A>C
ENST00000568472.6:n.661A>C
ENST00000568497.6:c.-185A>C ENSP00000456414.2:n.-185A>C
ENST00000568558.6:c.488A>C ENSP00000455603.2:p.Lys163Thr
ENST00000569430.7:c.785A>C ENSP00000454229.1:p.Lys262Thr
ENST00000628023.3:c.*81A>C ENSP00000486178.1:n.*81A>C
ENST00000635861.1:c.*309A>C ENSP00000490034.1:n.*309A>C
ENST00000635887.1:c.785A>C ENSP00000490709.1:p.Lys262Thr
ENST00000635958.1:n.896A>C
ENST00000635973.1:c.536A>C ENSP00000490363.1:p.Lys179Thr
ENST00000636017.1:c.*309A>C ENSP00000490538.1:n.*309A>C
ENST00000636078.1:n.827A>C
ENST00000636147.2:c.785A>C MANE Select ENSP00000490105.1:p.Lys262Thr
ENST00000636172.1:c.*309A>C ENSP00000490505.1:n.*309A>C
ENST00000636228.1:c.479A>C ENSP00000489627.1:p.Lys160Thr
ENST00000636351.1:n.505A>C
ENST00000636503.1:c.785A>C ENSP00000489824.1:p.Lys262Thr
ENST00000636685.1:n.292A>C
ENST00000636766.1:c.785A>C ENSP00000489841.1:p.Lys262Thr
ENST00000636839.1:n.937A>C
ENST00000636853.1:n.1700A>C
ENST00000636866.1:c.785A>C ENSP00000490880.1:p.Lys262Thr
ENST00000636907.1:n.936A>C
ENST00000636977.1:n.1853A>C
ENST00000637050.1:n.872A>C
ENST00000637100.1:c.785A>C ENSP00000490394.1:p.Lys262Thr
ENST00000637107.1:c.*309A>C ENSP00000490248.1:n.*309A>C
ENST00000637184.1:c.785A>C ENSP00000489952.1:p.Lys262Thr
ENST00000637299.1:c.*594A>C ENSP00000489823.1:n.*594A>C
ENST00000637376.1:c.785A>C ENSP00000490758.1:p.Lys262Thr
ENST00000637578.1:c.*309A>C ENSP00000490206.1:n.*309A>C
ENST00000637699.1:c.568A>C ENSP00000490049.1:n.568A>C
ENST00000637745.1:c.124A>C
ENST00000637871.1:c.*309A>C ENSP00000490670.1:n.*309A>C
ENST00000333496.13:c.713A>C ENSP00000329171.9:p.Lys238Thr
ENST00000355477.9:c.*22A>C ENSP00000347660.6:n.*22A>C
ENST00000357806.11:c.488A>C ENSP00000350457.7:p.Lys163Thr
ENST00000357857.13:c.623A>C ENSP00000350523.9:p.Lys208Thr
ENST00000359984.11:c.479A>C ENSP00000353073.8:p.Lys160Thr
ENST00000360019.6:c.785A>C ENSP00000353116.2:p.Lys262Thr
ENST00000395653.8:c.485A>C ENSP00000379014.4:p.Lys162Thr
ENST00000561689.5:n.626A>C
ENST00000563874.5:n.2139A>C
ENST00000564574.5:n.833A>C
ENST00000565047.1:n.379A>C
ENST00000565140.5:c.568A>C ENSP00000455342.1:n.568A>C
ENST00000565316.5:c.785A>C ENSP00000456117.1:p.Lys262Thr
ENST00000565354.5:n.4A>C
ENST00000565778.5:c.416A>C ENSP00000458015.1:p.Lys139Thr
ENST00000566057.5:c.399A>C ENSP00000456693.1:n.399A>C
ENST00000566083.5:n.1016A>C
ENST00000566824.5:n.834A>C
ENST00000567495.5:c.*22A>C ENSP00000456013.1:n.*22A>C
ENST00000567963.5:c.785A>C ENSP00000455387.1:p.Lys262Thr
ENST00000568076.5:n.568A>C
ENST00000568224.4:c.551A>C ENSP00000454253.1:p.Lys184Thr
ENST00000568422.5:c.*22A>C ENSP00000455549.1:n.*22A>C
ENST00000568452.5:n.785A>C
ENST00000568472.5:n.265A>C
ENST00000568497.5:c.*81A>C ENSP00000456414.1:n.*81A>C
ENST00000568558.5:c.326A>C ENSP00000455603.1:p.Lys109Thr
ENST00000569030.5:c.461-1339A>C ENSP00000454680.1:n.461-1339A>C
ENST00000569430.5:c.785A>C ENSP00000454229.1:p.Lys262Thr
ENST00000628023.2:c.*81A>C ENSP00000486178.1:n.*81A>C
ENST00000631023.2:c.785A>C ENSP00000486616.1:p.Lys262Thr
NM_000086.2:c.785A>C , LRG_689t1:c.785A>C NP_000077.1:p.Lys262Thr
NM_001042432.1:c.785A>C , LRG_689t2:c.785A>C NP_001035897.1:p.Lys262Thr
NM_001286104.1:c.713A>C NP_001273033.1:p.Lys238Thr
NM_001286105.1:c.485A>C NP_001273034.1:p.Lys162Thr
NM_001286109.1:c.551A>C NP_001273038.1:p.Lys184Thr
NM_001286110.1:c.623A>C NP_001273039.1:p.Lys208Thr
NM_001042432.2:c.785A>C MANE Select NP_001035897.1:p.Lys262Thr
NM_001286104.2:c.713A>C NP_001273033.1:p.Lys238Thr
NM_001286105.2:c.485A>C NP_001273034.1:p.Lys162Thr
NM_001286109.2:c.551A>C NP_001273038.1:p.Lys184Thr
NM_001286110.2:c.623A>C NP_001273039.1:p.Lys208Thr