Canonical Allele Identifier: CA395344096

Gene: CLN3

Linked Data

• MyVariant Identifiers: chr16:g.28493467A>C (hg19) ; chr16:g.28482146A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28482146A>C , CM000678.2:g.28482146A>C	GRCh38
NC_000016.9:g.28493467A>C , CM000678.1:g.28493467A>C	GRCh37
NC_000016.8:g.28400968A>C	NCBI36
NG_008654.2:g.15157T>G , LRG_689:g.15157T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333496.14:c.943T>G	ENSP00000329171.9:p.Cys315Gly
ENST00000355477.10:c.871T>G	ENSP00000347660.7:p.Cys291Gly
ENST00000357857.14:c.853T>G	ENSP00000350523.9:p.Cys285Gly
ENST00000359984.12:c.1015T>G	ENSP00000353073.9:p.Cys339Gly
ENST00000360019.8:c.943T>G	ENSP00000353116.3:p.Cys315Gly
ENST00000395653.9:c.556T>G	ENSP00000379014.5:p.Cys186Gly
ENST00000561689.6:n.1428T>G
ENST00000564091.6:c.355T>G	ENSP00000454466.2:p.Cys119Gly
ENST00000565316.6:c.964T>G	ENSP00000456117.1:p.Cys322Gly
ENST00000566824.6:n.1075T>G
ENST00000567963.6:c.853T>G	ENSP00000455387.2:p.Cys285Gly
ENST00000568076.6:n.1444T>G
ENST00000568422.6:c.*252T>G	ENSP00000455549.2:n.*252T>G
ENST00000568452.6:n.1246T>G
ENST00000568497.6:c.46T>G	ENSP00000456414.2:p.Cys16Gly
ENST00000569430.7:c.1015T>G	ENSP00000454229.1:p.Cys339Gly
ENST00000628023.3:c.*311T>G	ENSP00000486178.1:n.*311T>G
ENST00000635861.1:c.*667T>G	ENSP00000490034.1:n.*667T>G
ENST00000635887.1:c.1015T>G	ENSP00000490709.1:p.Cys339Gly
ENST00000635958.1:n.1300T>G
ENST00000635973.1:c.766T>G	ENSP00000490363.1:p.Cys256Gly
ENST00000636017.1:c.*539T>G	ENSP00000490538.1:n.*539T>G
ENST00000636078.1:n.1137T>G
ENST00000636147.2:c.1015T>G MANE Select	ENSP00000490105.1:p.Cys339Gly
ENST00000636172.1:c.*539T>G	ENSP00000490505.1:n.*539T>G
ENST00000636228.1:c.709T>G	ENSP00000489627.1:p.Cys237Gly
ENST00000636351.1:n.909T>G
ENST00000636503.1:c.1015T>G	ENSP00000489824.1:p.Cys339Gly
ENST00000636685.1:n.696T>G
ENST00000636766.1:c.1015T>G	ENSP00000489841.1:p.Cys339Gly
ENST00000636839.1:n.1389T>G
ENST00000636853.1:n.1930T>G
ENST00000636866.1:c.1015T>G	ENSP00000490880.1:p.Cys339Gly
ENST00000636907.1:n.1166T>G
ENST00000636977.1:n.2385T>G
ENST00000637050.1:n.1404T>G
ENST00000637100.1:c.964T>G	ENSP00000490394.1:p.Cys322Gly
ENST00000637107.1:c.*539T>G	ENSP00000490248.1:n.*539T>G
ENST00000637184.1:c.1015T>G	ENSP00000489952.1:p.Cys339Gly
ENST00000637299.1:c.*824T>G	ENSP00000489823.1:n.*824T>G
ENST00000637376.1:c.1015T>G	ENSP00000490758.1:p.Cys339Gly
ENST00000637378.1:c.187T>G	ENSP00000490831.1:p.Cys63Gly
ENST00000637578.1:c.*539T>G	ENSP00000490206.1:n.*539T>G
ENST00000637699.1:c.926T>G	ENSP00000490049.1:n.926T>G
ENST00000637745.1:c.354T>G
ENST00000637871.1:c.*713T>G	ENSP00000490670.1:n.*713T>G
ENST00000638036.1:c.177T>G
ENST00000333496.13:c.943T>G	ENSP00000329171.9:p.Cys315Gly
ENST00000355477.9:c.*252T>G	ENSP00000347660.6:n.*252T>G
ENST00000357806.11:c.718T>G	ENSP00000350457.7:p.Cys240Gly
ENST00000357857.13:c.853T>G	ENSP00000350523.9:p.Cys285Gly
ENST00000359984.11:c.709T>G	ENSP00000353073.8:p.Cys237Gly
ENST00000360019.6:c.1015T>G	ENSP00000353116.2:p.Cys339Gly
ENST00000395653.8:c.715T>G	ENSP00000379014.4:p.Cys239Gly
ENST00000561689.5:n.984T>G
ENST00000563874.5:n.2543T>G
ENST00000564091.5:c.104T>G
ENST00000565140.5:c.798T>G	ENSP00000455342.1:n.798T>G
ENST00000565316.5:c.964T>G	ENSP00000456117.1:p.Cys322Gly
ENST00000565354.5:n.328T>G
ENST00000566057.5:c.629T>G	ENSP00000456693.1:n.629T>G
ENST00000567963.5:c.906+331T>G	ENSP00000455387.1:n.906+331T>G
ENST00000568076.5:n.926T>G
ENST00000568224.4:c.781T>G	ENSP00000454253.1:p.Cys261Gly
ENST00000568422.5:c.*252T>G	ENSP00000455549.1:n.*252T>G
ENST00000568452.5:n.1143T>G
ENST00000569030.5:c.685T>G	ENSP00000454680.1:p.Cys229Gly
ENST00000569430.5:c.1015T>G	ENSP00000454229.1:p.Cys339Gly
ENST00000628023.2:c.*311T>G	ENSP00000486178.1:n.*311T>G
ENST00000631023.2:c.906+331T>G	ENSP00000486616.1:n.906+331T>G
NM_000086.2:c.1015T>G , LRG_689t1:c.1015T>G	NP_000077.1:p.Cys339Gly
NM_001042432.1:c.1015T>G , LRG_689t2:c.1015T>G	NP_001035897.1:p.Cys339Gly
NM_001286104.1:c.943T>G	NP_001273033.1:p.Cys315Gly
NM_001286105.1:c.715T>G	NP_001273034.1:p.Cys239Gly
NM_001286109.1:c.781T>G	NP_001273038.1:p.Cys261Gly
NM_001286110.1:c.853T>G	NP_001273039.1:p.Cys285Gly
NM_001042432.2:c.1015T>G MANE Select	NP_001035897.1:p.Cys339Gly
NM_001286104.2:c.943T>G	NP_001273033.1:p.Cys315Gly
NM_001286105.2:c.715T>G	NP_001273034.1:p.Cys239Gly
NM_001286109.2:c.781T>G	NP_001273038.1:p.Cys261Gly
NM_001286110.2:c.853T>G	NP_001273039.1:p.Cys285Gly