Canonical Allele Identifier: CA494268718
Gene: CLN3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.28493438C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28482117C>G , CM000678.2:g.28482117C>G GRCh38
NC_000016.9:g.28493438C>G , CM000678.1:g.28493438C>G GRCh37
NC_000016.8:g.28400939C>G NCBI36
NG_008654.2:g.15186G>C , LRG_689:g.15186G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333496.14:c.972G>C ENSP00000329171.9:p.Leu324=
ENST00000355477.10:c.900G>C ENSP00000347660.7:p.Leu300=
ENST00000357857.14:c.882G>C ENSP00000350523.9:p.Leu294=
ENST00000359984.12:c.1044G>C ENSP00000353073.9:p.Leu348=
ENST00000360019.8:c.972G>C ENSP00000353116.3:p.Leu324=
ENST00000395653.9:c.585G>C ENSP00000379014.5:p.Leu195=
ENST00000561689.6:n.1457G>C
ENST00000564091.6:c.384G>C ENSP00000454466.2:p.Leu128=
ENST00000565316.6:c.993G>C ENSP00000456117.1:p.Leu331=
ENST00000566824.6:n.1104G>C
ENST00000567963.6:c.882G>C ENSP00000455387.2:p.Leu294=
ENST00000568076.6:n.1473G>C
ENST00000568422.6:c.*281G>C ENSP00000455549.2:n.*281G>C
ENST00000568452.6:n.1275G>C
ENST00000568497.6:c.75G>C ENSP00000456414.2:p.Leu25=
ENST00000569430.7:c.1044G>C ENSP00000454229.1:p.Leu348=
ENST00000628023.3:c.*340G>C ENSP00000486178.1:n.*340G>C
ENST00000635861.1:c.*696G>C ENSP00000490034.1:n.*696G>C
ENST00000635887.1:c.1044G>C ENSP00000490709.1:p.Leu348=
ENST00000635958.1:n.1329G>C
ENST00000635973.1:c.795G>C ENSP00000490363.1:p.Leu265=
ENST00000636017.1:c.*568G>C ENSP00000490538.1:n.*568G>C
ENST00000636078.1:n.1166G>C
ENST00000636147.2:c.1044G>C MANE Select ENSP00000490105.1:p.Leu348=
ENST00000636172.1:c.*568G>C ENSP00000490505.1:n.*568G>C
ENST00000636228.1:c.738G>C ENSP00000489627.1:p.Leu246=
ENST00000636351.1:n.938G>C
ENST00000636503.1:c.1044G>C ENSP00000489824.1:p.Leu348=
ENST00000636685.1:n.725G>C
ENST00000636766.1:c.1044G>C ENSP00000489841.1:p.Leu348=
ENST00000636839.1:n.1418G>C
ENST00000636853.1:n.1959G>C
ENST00000636866.1:c.1044G>C ENSP00000490880.1:p.Leu348=
ENST00000636907.1:n.1195G>C
ENST00000636977.1:n.2414G>C
ENST00000637050.1:n.1433G>C
ENST00000637100.1:c.993G>C ENSP00000490394.1:p.Leu331=
ENST00000637107.1:c.*568G>C ENSP00000490248.1:n.*568G>C
ENST00000637184.1:c.1044G>C ENSP00000489952.1:p.Leu348=
ENST00000637299.1:c.*853G>C ENSP00000489823.1:n.*853G>C
ENST00000637376.1:c.1044G>C ENSP00000490758.1:p.Leu348=
ENST00000637378.1:c.216G>C ENSP00000490831.1:p.Leu72=
ENST00000637578.1:c.*568G>C ENSP00000490206.1:n.*568G>C
ENST00000637699.1:c.955G>C ENSP00000490049.1:n.955G>C
ENST00000637745.1:c.383G>C
ENST00000637871.1:c.*742G>C ENSP00000490670.1:n.*742G>C
ENST00000638036.1:c.206G>C
ENST00000333496.13:c.972G>C ENSP00000329171.9:p.Leu324=
ENST00000355477.9:c.*281G>C ENSP00000347660.6:n.*281G>C
ENST00000357806.11:c.747G>C ENSP00000350457.7:p.Leu249=
ENST00000357857.13:c.882G>C ENSP00000350523.9:p.Leu294=
ENST00000359984.11:c.738G>C ENSP00000353073.8:p.Leu246=
ENST00000360019.6:c.1044G>C ENSP00000353116.2:p.Leu348=
ENST00000395653.8:c.744G>C ENSP00000379014.4:p.Leu248=
ENST00000561689.5:n.1013G>C
ENST00000563874.5:n.2572G>C
ENST00000564091.5:c.133G>C
ENST00000565140.5:c.827G>C ENSP00000455342.1:n.827G>C
ENST00000565316.5:c.993G>C ENSP00000456117.1:p.Leu331=
ENST00000565354.5:n.357G>C
ENST00000566057.5:c.658G>C ENSP00000456693.1:n.658G>C
ENST00000567963.5:c.906+360G>C ENSP00000455387.1:n.906+360G>C
ENST00000568076.5:n.955G>C
ENST00000568224.4:c.810G>C ENSP00000454253.1:p.Leu270=
ENST00000568422.5:c.*281G>C ENSP00000455549.1:n.*281G>C
ENST00000568452.5:n.1172G>C
ENST00000569030.5:c.714G>C ENSP00000454680.1:p.Leu238=
ENST00000569430.5:c.1044G>C ENSP00000454229.1:p.Leu348=
ENST00000628023.2:c.*340G>C ENSP00000486178.1:n.*340G>C
ENST00000631023.2:c.906+360G>C ENSP00000486616.1:n.906+360G>C
NM_000086.2:c.1044G>C , LRG_689t1:c.1044G>C NP_000077.1:p.Leu348=
NM_001042432.1:c.1044G>C , LRG_689t2:c.1044G>C NP_001035897.1:p.Leu348=
NM_001286104.1:c.972G>C NP_001273033.1:p.Leu324=
NM_001286105.1:c.744G>C NP_001273034.1:p.Leu248=
NM_001286109.1:c.810G>C NP_001273038.1:p.Leu270=
NM_001286110.1:c.882G>C NP_001273039.1:p.Leu294=
NM_001042432.2:c.1044G>C MANE Select NP_001035897.1:p.Leu348=
NM_001286104.2:c.972G>C NP_001273033.1:p.Leu324=
NM_001286105.2:c.744G>C NP_001273034.1:p.Leu248=
NM_001286109.2:c.810G>C NP_001273038.1:p.Leu270=
NM_001286110.2:c.882G>C NP_001273039.1:p.Leu294=