Canonical Allele Identifier: CA2215691577

Gene: CLN3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28477739C= , CM000678.2:g.28477739C=	GRCh38
NC_000016.9:g.28489060C= , CM000678.1:g.28489060C=	GRCh37
NC_000016.8:g.28396561C=	NCBI36
NG_008654.2:g.19564G= , LRG_689:g.19564G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333496.14:c.1123G=	ENSP00000329171.9:p.Glu375=
ENST00000355477.10:c.1051G=	ENSP00000347660.7:p.Glu351=
ENST00000357857.14:c.1033G=	ENSP00000350523.9:p.Glu345=
ENST00000359984.12:c.1195G=	ENSP00000353073.9:p.Glu399=
ENST00000360019.8:c.1123G=	ENSP00000353116.3:p.Glu375=
ENST00000395653.9:c.736G=	ENSP00000379014.5:p.Glu246=
ENST00000561689.6:n.1608G=
ENST00000564091.6:c.535G=	ENSP00000454466.2:p.Glu179=
ENST00000565316.6:c.1144G=	ENSP00000456117.1:p.Glu382=
ENST00000567963.6:c.1033G=	ENSP00000455387.2:p.Glu345=
ENST00000568076.6:n.1624G=
ENST00000568422.6:c.*432G=	ENSP00000455549.2:n.*432G=
ENST00000568452.6:n.1426G=
ENST00000569430.7:c.1195G=	ENSP00000454229.1:p.Glu399=
ENST00000628023.3:c.*491G=	ENSP00000486178.1:n.*491G=
ENST00000635861.1:c.*847G=	ENSP00000490034.1:n.*847G=
ENST00000635887.1:c.1195G=	ENSP00000490709.1:p.Glu399=
ENST00000635958.1:n.1602G=
ENST00000636017.1:c.*719G=	ENSP00000490538.1:n.*719G=
ENST00000636078.1:n.1317G=
ENST00000636147.2:c.1195G= MANE Select	ENSP00000490105.1:p.Glu399=
ENST00000636172.1:c.*719G=	ENSP00000490505.1:n.*719G=
ENST00000636228.1:c.889G=	ENSP00000489627.1:p.Glu297=
ENST00000636351.1:n.1089G=
ENST00000636503.1:c.*225G=	ENSP00000489824.1:n.*225G=
ENST00000636766.1:c.1195G=	ENSP00000489841.1:p.Glu399=
ENST00000636839.1:n.1691G=
ENST00000636853.1:n.2208G=
ENST00000636866.1:c.1195G=	ENSP00000490880.1:p.Glu399=
ENST00000636907.1:n.1346G=
ENST00000636977.1:n.2687G=
ENST00000637050.1:n.1584G=
ENST00000637100.1:c.1006-3477G=	ENSP00000490394.1:n.1006-3477G=
ENST00000637107.1:c.*719G=	ENSP00000490248.1:n.*719G=
ENST00000637184.1:c.*225G=	ENSP00000489952.1:n.*225G=
ENST00000637299.1:c.*1004G=	ENSP00000489823.1:n.*1004G=
ENST00000637376.1:c.*225G=	ENSP00000490758.1:n.*225G=
ENST00000637378.1:c.228+4366G=	ENSP00000490831.1:n.228+4366G=
ENST00000637578.1:c.*719G=	ENSP00000490206.1:n.*719G=
ENST00000637699.1:c.1106G=	ENSP00000490049.1:n.1106G=
ENST00000637745.1:c.632G=
ENST00000637871.1:c.*893G=	ENSP00000490670.1:n.*893G=
ENST00000638036.1:c.357G=
ENST00000333496.13:c.1123G=	ENSP00000329171.9:p.Glu375=
ENST00000355477.9:c.*432G=	ENSP00000347660.6:n.*432G=
ENST00000357806.11:c.898G=	ENSP00000350457.7:p.Glu300=
ENST00000357857.13:c.1033G=	ENSP00000350523.9:p.Glu345=
ENST00000359984.11:c.889G=	ENSP00000353073.8:p.Glu297=
ENST00000360019.6:c.1195G=	ENSP00000353116.2:p.Glu399=
ENST00000395653.8:c.895G=	ENSP00000379014.4:p.Glu299=
ENST00000561689.5:n.1164G=
ENST00000563874.5:n.2723G=
ENST00000564091.5:c.284G=
ENST00000565140.5:c.1103G=	ENSP00000455342.1:n.1103G=
ENST00000565316.5:c.1144G=	ENSP00000456117.1:p.Glu382=
ENST00000565354.5:n.508G=
ENST00000566057.5:c.809G=	ENSP00000456693.1:n.809G=
ENST00000567963.5:c.907-104G=	ENSP00000455387.1:n.907-104G=
ENST00000568076.5:n.1106G=
ENST00000568224.4:c.961G=	ENSP00000454253.1:p.Glu321=
ENST00000568422.5:c.*432G=	ENSP00000455549.1:n.*432G=
ENST00000568452.5:n.1323G=
ENST00000569030.5:c.987G=	ENSP00000454680.1:n.987G=
ENST00000569430.5:c.1195G=	ENSP00000454229.1:p.Glu399=
ENST00000628023.2:c.*491G=	ENSP00000486178.1:n.*491G=
ENST00000631023.2:c.907-104G=	ENSP00000486616.1:n.907-104G=
NM_000086.2:c.1195G= , LRG_689t1:c.1195G=	NP_000077.1:p.Glu399=
NM_001042432.1:c.1195G= , LRG_689t2:c.1195G=	NP_001035897.1:p.Glu399=
NM_001286104.1:c.1123G=	NP_001273033.1:p.Glu375=
NM_001286105.1:c.895G=	NP_001273034.1:p.Glu299=
NM_001286109.1:c.961G=	NP_001273038.1:p.Glu321=
NM_001286110.1:c.1033G=	NP_001273039.1:p.Glu345=
NM_001042432.2:c.1195G= MANE Select	NP_001035897.1:p.Glu399=
NM_001286104.2:c.1123G=	NP_001273033.1:p.Glu375=
NM_001286105.2:c.895G=	NP_001273034.1:p.Glu299=
NM_001286109.2:c.961G=	NP_001273038.1:p.Glu321=
NM_001286110.2:c.1033G=	NP_001273039.1:p.Glu345=