Canonical Allele Identifier: CA395344124

Gene: CLN3

Linked Data

• MyVariant Identifiers: chr16:g.28493473G>A (hg19) ; chr16:g.28482152G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28482152G>A , CM000678.2:g.28482152G>A	GRCh38
NC_000016.9:g.28493473G>A , CM000678.1:g.28493473G>A	GRCh37
NC_000016.8:g.28400974G>A	NCBI36
NG_008654.2:g.15151C>T , LRG_689:g.15151C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333496.14:c.937C>T	ENSP00000329171.9:p.Leu313Phe
ENST00000355477.10:c.865C>T	ENSP00000347660.7:p.Leu289Phe
ENST00000357857.14:c.847C>T	ENSP00000350523.9:p.Leu283Phe
ENST00000359984.12:c.1009C>T	ENSP00000353073.9:p.Leu337Phe
ENST00000360019.8:c.937C>T	ENSP00000353116.3:p.Leu313Phe
ENST00000395653.9:c.550C>T	ENSP00000379014.5:p.Leu184Phe
ENST00000561689.6:n.1422C>T
ENST00000564091.6:c.349C>T	ENSP00000454466.2:p.Leu117Phe
ENST00000565316.6:c.958C>T	ENSP00000456117.1:p.Leu320Phe
ENST00000566824.6:n.1069C>T
ENST00000567963.6:c.847C>T	ENSP00000455387.2:p.Leu283Phe
ENST00000568076.6:n.1438C>T
ENST00000568422.6:c.*246C>T	ENSP00000455549.2:n.*246C>T
ENST00000568452.6:n.1240C>T
ENST00000568497.6:c.40C>T	ENSP00000456414.2:p.Leu14Phe
ENST00000569430.7:c.1009C>T	ENSP00000454229.1:p.Leu337Phe
ENST00000628023.3:c.*305C>T	ENSP00000486178.1:n.*305C>T
ENST00000635861.1:c.*661C>T	ENSP00000490034.1:n.*661C>T
ENST00000635887.1:c.1009C>T	ENSP00000490709.1:p.Leu337Phe
ENST00000635958.1:n.1294C>T
ENST00000635973.1:c.760C>T	ENSP00000490363.1:p.Leu254Phe
ENST00000636017.1:c.*533C>T	ENSP00000490538.1:n.*533C>T
ENST00000636078.1:n.1131C>T
ENST00000636147.2:c.1009C>T MANE Select	ENSP00000490105.1:p.Leu337Phe
ENST00000636172.1:c.*533C>T	ENSP00000490505.1:n.*533C>T
ENST00000636228.1:c.703C>T	ENSP00000489627.1:p.Leu235Phe
ENST00000636351.1:n.903C>T
ENST00000636503.1:c.1009C>T	ENSP00000489824.1:p.Leu337Phe
ENST00000636685.1:n.690C>T
ENST00000636766.1:c.1009C>T	ENSP00000489841.1:p.Leu337Phe
ENST00000636839.1:n.1383C>T
ENST00000636853.1:n.1924C>T
ENST00000636866.1:c.1009C>T	ENSP00000490880.1:p.Leu337Phe
ENST00000636907.1:n.1160C>T
ENST00000636977.1:n.2379C>T
ENST00000637050.1:n.1398C>T
ENST00000637100.1:c.958C>T	ENSP00000490394.1:p.Leu320Phe
ENST00000637107.1:c.*533C>T	ENSP00000490248.1:n.*533C>T
ENST00000637184.1:c.1009C>T	ENSP00000489952.1:p.Leu337Phe
ENST00000637299.1:c.*818C>T	ENSP00000489823.1:n.*818C>T
ENST00000637376.1:c.1009C>T	ENSP00000490758.1:p.Leu337Phe
ENST00000637378.1:c.181C>T	ENSP00000490831.1:p.Leu61Phe
ENST00000637578.1:c.*533C>T	ENSP00000490206.1:n.*533C>T
ENST00000637699.1:c.920C>T	ENSP00000490049.1:n.920C>T
ENST00000637745.1:c.348C>T
ENST00000637871.1:c.*707C>T	ENSP00000490670.1:n.*707C>T
ENST00000638036.1:c.171C>T
ENST00000333496.13:c.937C>T	ENSP00000329171.9:p.Leu313Phe
ENST00000355477.9:c.*246C>T	ENSP00000347660.6:n.*246C>T
ENST00000357806.11:c.712C>T	ENSP00000350457.7:p.Leu238Phe
ENST00000357857.13:c.847C>T	ENSP00000350523.9:p.Leu283Phe
ENST00000359984.11:c.703C>T	ENSP00000353073.8:p.Leu235Phe
ENST00000360019.6:c.1009C>T	ENSP00000353116.2:p.Leu337Phe
ENST00000395653.8:c.709C>T	ENSP00000379014.4:p.Leu237Phe
ENST00000561689.5:n.978C>T
ENST00000563874.5:n.2537C>T
ENST00000564091.5:c.98C>T
ENST00000565140.5:c.792C>T	ENSP00000455342.1:n.792C>T
ENST00000565316.5:c.958C>T	ENSP00000456117.1:p.Leu320Phe
ENST00000565354.5:n.322C>T
ENST00000566057.5:c.623C>T	ENSP00000456693.1:n.623C>T
ENST00000567963.5:c.906+325C>T	ENSP00000455387.1:n.906+325C>T
ENST00000568076.5:n.920C>T
ENST00000568224.4:c.775C>T	ENSP00000454253.1:p.Leu259Phe
ENST00000568422.5:c.*246C>T	ENSP00000455549.1:n.*246C>T
ENST00000568452.5:n.1137C>T
ENST00000568558.5:c.550C>T	ENSP00000455603.1:p.Leu184Phe
ENST00000569030.5:c.679C>T	ENSP00000454680.1:p.Leu227Phe
ENST00000569430.5:c.1009C>T	ENSP00000454229.1:p.Leu337Phe
ENST00000628023.2:c.*305C>T	ENSP00000486178.1:n.*305C>T
ENST00000631023.2:c.906+325C>T	ENSP00000486616.1:n.906+325C>T
NM_000086.2:c.1009C>T , LRG_689t1:c.1009C>T	NP_000077.1:p.Leu337Phe
NM_001042432.1:c.1009C>T , LRG_689t2:c.1009C>T	NP_001035897.1:p.Leu337Phe
NM_001286104.1:c.937C>T	NP_001273033.1:p.Leu313Phe
NM_001286105.1:c.709C>T	NP_001273034.1:p.Leu237Phe
NM_001286109.1:c.775C>T	NP_001273038.1:p.Leu259Phe
NM_001286110.1:c.847C>T	NP_001273039.1:p.Leu283Phe
NM_001042432.2:c.1009C>T MANE Select	NP_001035897.1:p.Leu337Phe
NM_001286104.2:c.937C>T	NP_001273033.1:p.Leu313Phe
NM_001286105.2:c.709C>T	NP_001273034.1:p.Leu237Phe
NM_001286109.2:c.775C>T	NP_001273038.1:p.Leu259Phe
NM_001286110.2:c.847C>T	NP_001273039.1:p.Leu283Phe