Canonical Allele Identifier: CA10606047
Gene: CLN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 288316
dbSNP Id: rs147667964

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28486487G>C , CM000678.2:g.28486487G>C GRCh38
NC_000016.9:g.28497808G>C , CM000678.1:g.28497808G>C GRCh37
NC_000016.8:g.28405309G>C NCBI36
NG_008654.2:g.10816C>G , LRG_689:g.10816C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333496.14:c.465C>G ENSP00000329171.9:p.Ala155=
ENST00000355477.10:c.533+91C>G ENSP00000347660.7:n.533+91C>G
ENST00000357857.14:c.375C>G ENSP00000350523.9:p.Ala125=
ENST00000359984.12:c.537C>G ENSP00000353073.9:p.Ala179=
ENST00000360019.8:c.465C>G ENSP00000353116.3:p.Ala155=
ENST00000395653.9:c.218+969C>G ENSP00000379014.5:n.218+969C>G
ENST00000561505.2:c.*61C>G ENSP00000457615.2:n.*61C>G
ENST00000561689.6:n.822C>G
ENST00000565316.6:c.537C>G ENSP00000456117.1:p.Ala179=
ENST00000565778.6:c.308+969C>G ENSP00000458015.1:n.308+969C>G
ENST00000566083.6:n.995C>G
ENST00000566824.6:n.517C>G
ENST00000567495.6:c.464C>G ENSP00000456013.2:p.Pro155Arg
ENST00000567963.6:c.375C>G ENSP00000455387.2:p.Ala125=
ENST00000568076.6:n.664C>G
ENST00000568422.6:c.460+969C>G ENSP00000455549.2:n.460+969C>G
ENST00000568452.6:n.640C>G
ENST00000568472.6:n.553+969C>G
ENST00000568497.6:c.-292-2369C>G ENSP00000456414.2:n.-292-2369C>G
ENST00000568558.6:c.380+969C>G ENSP00000455603.2:n.380+969C>G
ENST00000569430.7:c.537C>G ENSP00000454229.1:p.Ala179=
ENST00000628023.3:c.223-2369C>G ENSP00000486178.1:n.223-2369C>G
ENST00000635861.1:c.*61C>G ENSP00000490034.1:n.*61C>G
ENST00000635887.1:c.537C>G ENSP00000490709.1:p.Ala179=
ENST00000635958.1:n.648C>G
ENST00000635973.1:c.288C>G ENSP00000490363.1:p.Ala96=
ENST00000636017.1:c.*61C>G ENSP00000490538.1:n.*61C>G
ENST00000636078.1:n.579C>G
ENST00000636147.2:c.537C>G MANE Select ENSP00000490105.1:p.Ala179=
ENST00000636172.1:c.*61C>G ENSP00000490505.1:n.*61C>G
ENST00000636228.1:c.371+91C>G ENSP00000489627.1:n.371+91C>G
ENST00000636351.1:n.257C>G
ENST00000636503.1:c.537C>G ENSP00000489824.1:p.Ala179=
ENST00000636766.1:c.537C>G ENSP00000489841.1:p.Ala179=
ENST00000636839.1:n.689C>G
ENST00000636853.1:n.1452C>G
ENST00000636866.1:c.537C>G ENSP00000490880.1:p.Ala179=
ENST00000636977.1:n.1605C>G
ENST00000637100.1:c.537C>G ENSP00000490394.1:p.Ala179=
ENST00000637107.1:c.*61C>G ENSP00000490248.1:n.*61C>G
ENST00000637184.1:c.537C>G ENSP00000489952.1:p.Ala179=
ENST00000637299.1:c.*346C>G ENSP00000489823.1:n.*346C>G
ENST00000637376.1:c.537C>G ENSP00000490758.1:p.Ala179=
ENST00000637578.1:c.*61C>G ENSP00000490206.1:n.*61C>G
ENST00000637699.1:c.460+969C>G ENSP00000490049.1:n.460+969C>G
ENST00000637871.1:c.*61C>G ENSP00000490670.1:n.*61C>G
ENST00000637985.1:c.*476C>G ENSP00000490932.1:n.*476C>G
ENST00000333496.13:c.465C>G ENSP00000329171.9:p.Ala155=
ENST00000355477.9:c.460+969C>G ENSP00000347660.6:n.460+969C>G
ENST00000357806.11:c.380+969C>G ENSP00000350457.7:n.380+969C>G
ENST00000357857.13:c.375C>G ENSP00000350523.9:p.Ala125=
ENST00000359984.11:c.371+91C>G ENSP00000353073.8:n.371+91C>G
ENST00000360019.6:c.537C>G ENSP00000353116.2:p.Ala179=
ENST00000395653.8:c.237C>G ENSP00000379014.4:p.Ala79=
ENST00000561505.1:c.237C>G ENSP00000457615.1:p.Ala79=
ENST00000561689.5:n.378C>G
ENST00000563874.5:n.1891C>G
ENST00000564574.5:n.585C>G
ENST00000565047.1:n.271+969C>G
ENST00000565140.5:c.460+969C>G ENSP00000455342.1:n.460+969C>G
ENST00000565316.5:c.537C>G ENSP00000456117.1:p.Ala179=
ENST00000565688.5:c.288C>G ENSP00000456122.1:p.Ala96=
ENST00000565778.5:c.308+969C>G ENSP00000458015.1:n.308+969C>G
ENST00000566057.5:c.291+969C>G ENSP00000456693.1:n.291+969C>G
ENST00000566083.5:n.768C>G
ENST00000566824.5:n.586C>G
ENST00000567495.5:c.460+969C>G ENSP00000456013.1:n.460+969C>G
ENST00000567963.5:c.537C>G ENSP00000455387.1:p.Ala179=
ENST00000568076.5:n.460+969C>G
ENST00000568224.4:c.303C>G ENSP00000454253.1:p.Ala101=
ENST00000568422.5:c.313+91C>G ENSP00000455549.1:n.313+91C>G
ENST00000568452.5:n.537C>G
ENST00000568472.5:n.158-2369C>G
ENST00000568497.5:c.223-2369C>G ENSP00000456414.1:n.223-2369C>G
ENST00000568558.5:c.218+969C>G ENSP00000455603.1:n.218+969C>G
ENST00000569030.5:c.460+969C>G ENSP00000454680.1:n.460+969C>G
ENST00000569430.5:c.537C>G ENSP00000454229.1:p.Ala179=
ENST00000628023.2:c.223-2369C>G ENSP00000486178.1:n.223-2369C>G
ENST00000631023.2:c.537C>G ENSP00000486616.1:p.Ala179=
NM_000086.2:c.537C>G , LRG_689t1:c.537C>G NP_000077.1:p.Ala179=
NM_001042432.1:c.537C>G , LRG_689t2:c.537C>G NP_001035897.1:p.Ala179=
NM_001286104.1:c.465C>G NP_001273033.1:p.Ala155=
NM_001286105.1:c.237C>G NP_001273034.1:p.Ala79=
NM_001286109.1:c.303C>G NP_001273038.1:p.Ala101=
NM_001286110.1:c.375C>G NP_001273039.1:p.Ala125=
NM_001042432.2:c.537C>G MANE Select NP_001035897.1:p.Ala179=
NM_001286104.2:c.465C>G NP_001273033.1:p.Ala155=
NM_001286105.2:c.237C>G NP_001273034.1:p.Ala79=
NM_001286109.2:c.303C>G NP_001273038.1:p.Ala101=
NM_001286110.2:c.375C>G NP_001273039.1:p.Ala125=