Canonical Allele Identifier: CA395344975

Gene: CLN3

Linked Data

• MyVariant Identifiers: chr16:g.28495439G>A (hg19) ; chr16:g.28484118G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28484118G>A , CM000678.2:g.28484118G>A	GRCh38
NC_000016.9:g.28495439G>A , CM000678.1:g.28495439G>A	GRCh37
NC_000016.8:g.28402940G>A	NCBI36
NG_008654.2:g.13185C>T , LRG_689:g.13185C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333496.14:c.606C>T	ENSP00000329171.9:p.Ser202=
ENST00000355477.10:c.534C>T	ENSP00000347660.7:p.Ser178=
ENST00000357857.14:c.516C>T	ENSP00000350523.9:p.Ser172=
ENST00000359984.12:c.678C>T	ENSP00000353073.9:p.Ser226=
ENST00000360019.8:c.606C>T	ENSP00000353116.3:p.Ser202=
ENST00000395653.9:c.219C>T	ENSP00000379014.5:p.Cys73=
ENST00000561689.6:n.963C>T
ENST00000564091.6:c.18C>T	ENSP00000454466.2:p.Ser6=
ENST00000565316.6:c.678C>T	ENSP00000456117.1:p.Ser226=
ENST00000565778.6:c.309C>T	ENSP00000458015.1:p.Cys103=
ENST00000566083.6:n.1136C>T
ENST00000566824.6:n.658C>T
ENST00000567495.6:c.*137C>T	ENSP00000456013.2:n.*137C>T
ENST00000567963.6:c.516C>T	ENSP00000455387.2:p.Ser172=
ENST00000568076.6:n.805C>T
ENST00000568422.6:c.461C>T	ENSP00000455549.2:p.Ala154Val
ENST00000568452.6:n.781C>T
ENST00000568472.6:n.554C>T
ENST00000568497.6:c.-292C>T	ENSP00000456414.2:n.-292C>T
ENST00000568558.6:c.381C>T	ENSP00000455603.2:p.Cys127=
ENST00000569430.7:c.678C>T	ENSP00000454229.1:p.Ser226=
ENST00000628023.3:c.223C>T	ENSP00000486178.1:p.Leu75=
ENST00000635861.1:c.*202C>T	ENSP00000490034.1:n.*202C>T
ENST00000635887.1:c.678C>T	ENSP00000490709.1:p.Ser226=
ENST00000635958.1:n.789C>T
ENST00000635973.1:c.429C>T	ENSP00000490363.1:p.Ser143=
ENST00000636017.1:c.*202C>T	ENSP00000490538.1:n.*202C>T
ENST00000636078.1:n.720C>T
ENST00000636147.2:c.678C>T MANE Select	ENSP00000490105.1:p.Ser226=
ENST00000636172.1:c.*202C>T	ENSP00000490505.1:n.*202C>T
ENST00000636228.1:c.372C>T	ENSP00000489627.1:p.Ser124=
ENST00000636351.1:n.398C>T
ENST00000636503.1:c.678C>T	ENSP00000489824.1:p.Ser226=
ENST00000636685.1:n.185C>T
ENST00000636766.1:c.678C>T	ENSP00000489841.1:p.Ser226=
ENST00000636839.1:n.830C>T
ENST00000636853.1:n.1593C>T
ENST00000636866.1:c.678C>T	ENSP00000490880.1:p.Ser226=
ENST00000636907.1:n.829C>T
ENST00000636977.1:n.1746C>T
ENST00000637050.1:n.765C>T
ENST00000637100.1:c.678C>T	ENSP00000490394.1:p.Ser226=
ENST00000637107.1:c.*202C>T	ENSP00000490248.1:n.*202C>T
ENST00000637184.1:c.678C>T	ENSP00000489952.1:p.Ser226=
ENST00000637299.1:c.*487C>T	ENSP00000489823.1:n.*487C>T
ENST00000637376.1:c.678C>T	ENSP00000490758.1:p.Ser226=
ENST00000637578.1:c.*202C>T	ENSP00000490206.1:n.*202C>T
ENST00000637699.1:c.461C>T	ENSP00000490049.1:p.Ala154Val
ENST00000637745.1:c.17C>T
ENST00000637871.1:c.*202C>T	ENSP00000490670.1:n.*202C>T
ENST00000333496.13:c.606C>T	ENSP00000329171.9:p.Ser202=
ENST00000355477.9:c.461C>T	ENSP00000347660.6:p.Ala154Val
ENST00000357806.11:c.381C>T	ENSP00000350457.7:p.Cys127=
ENST00000357857.13:c.516C>T	ENSP00000350523.9:p.Ser172=
ENST00000359984.11:c.372C>T	ENSP00000353073.8:p.Ser124=
ENST00000360019.6:c.678C>T	ENSP00000353116.2:p.Ser226=
ENST00000395653.8:c.378C>T	ENSP00000379014.4:p.Ser126=
ENST00000561689.5:n.519C>T
ENST00000563874.5:n.2032C>T
ENST00000564574.5:n.726C>T
ENST00000565047.1:n.272C>T
ENST00000565140.5:c.461C>T	ENSP00000455342.1:p.Ala154Val
ENST00000565316.5:c.678C>T	ENSP00000456117.1:p.Ser226=
ENST00000565688.5:c.429C>T	ENSP00000456122.1:p.Ser143=
ENST00000565778.5:c.309C>T	ENSP00000458015.1:p.Cys103=
ENST00000566057.5:c.292C>T	ENSP00000456693.1:p.Leu98=
ENST00000566083.5:n.909C>T
ENST00000566824.5:n.727C>T
ENST00000567495.5:c.461C>T	ENSP00000456013.1:p.Ala154Val
ENST00000567963.5:c.678C>T	ENSP00000455387.1:p.Ser226=
ENST00000568076.5:n.461C>T
ENST00000568224.4:c.444C>T	ENSP00000454253.1:p.Ser148=
ENST00000568422.5:c.314C>T	ENSP00000455549.1:p.Ala105Val
ENST00000568452.5:n.678C>T
ENST00000568472.5:n.158C>T
ENST00000568497.5:c.223C>T	ENSP00000456414.1:p.Leu75=
ENST00000568558.5:c.219C>T	ENSP00000455603.1:p.Cys73=
ENST00000569030.5:c.461-1446C>T	ENSP00000454680.1:n.461-1446C>T
ENST00000569430.5:c.678C>T	ENSP00000454229.1:p.Ser226=
ENST00000628023.2:c.223C>T	ENSP00000486178.1:p.Leu75=
ENST00000631023.2:c.678C>T	ENSP00000486616.1:p.Ser226=
NM_000086.2:c.678C>T , LRG_689t1:c.678C>T	NP_000077.1:p.Ser226=
NM_001042432.1:c.678C>T , LRG_689t2:c.678C>T	NP_001035897.1:p.Ser226=
NM_001286104.1:c.606C>T	NP_001273033.1:p.Ser202=
NM_001286105.1:c.378C>T	NP_001273034.1:p.Ser126=
NM_001286109.1:c.444C>T	NP_001273038.1:p.Ser148=
NM_001286110.1:c.516C>T	NP_001273039.1:p.Ser172=
NM_001042432.2:c.678C>T MANE Select	NP_001035897.1:p.Ser226=
NM_001286104.2:c.606C>T	NP_001273033.1:p.Ser202=
NM_001286105.2:c.378C>T	NP_001273034.1:p.Ser126=
NM_001286109.2:c.444C>T	NP_001273038.1:p.Ser148=
NM_001286110.2:c.516C>T	NP_001273039.1:p.Ser172=