Canonical Allele Identifier: CA494271991

Gene: CLN3

Linked Data

• MyVariant Identifiers: chr16:g.28495343G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28484022G>C , CM000678.2:g.28484022G>C	GRCh38
NC_000016.9:g.28495343G>C , CM000678.1:g.28495343G>C	GRCh37
NC_000016.8:g.28402844G>C	NCBI36
NG_008654.2:g.13281C>G , LRG_689:g.13281C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000333496.14:c.702C>G	ENSP00000329171.9:p.Ala234=
ENST00000355477.10:c.630C>G	ENSP00000347660.7:p.Ala210=
ENST00000357857.14:c.612C>G	ENSP00000350523.9:p.Ala204=
ENST00000359984.12:c.774C>G	ENSP00000353073.9:p.Ala258=
ENST00000360019.8:c.702C>G	ENSP00000353116.3:p.Ala234=
ENST00000395653.9:c.315C>G	ENSP00000379014.5:p.Ala105=
ENST00000561689.6:n.1059C>G
ENST00000564091.6:c.114C>G	ENSP00000454466.2:p.Ala38=
ENST00000565316.6:c.774C>G	ENSP00000456117.1:p.Ala258=
ENST00000565778.6:c.405C>G	ENSP00000458015.1:p.Ala135=
ENST00000566083.6:n.1232C>G
ENST00000566824.6:n.754C>G
ENST00000567963.6:c.612C>G	ENSP00000455387.2:p.Ala204=
ENST00000568076.6:n.901C>G
ENST00000568422.6:c.*11C>G	ENSP00000455549.2:n.*11C>G
ENST00000568452.6:n.877C>G
ENST00000568472.6:n.650C>G
ENST00000568497.6:c.-196C>G	ENSP00000456414.2:n.-196C>G
ENST00000568558.6:c.477C>G	ENSP00000455603.2:p.Ala159=
ENST00000569430.7:c.774C>G	ENSP00000454229.1:p.Ala258=
ENST00000628023.3:c.*70C>G	ENSP00000486178.1:n.*70C>G
ENST00000635861.1:c.*298C>G	ENSP00000490034.1:n.*298C>G
ENST00000635887.1:c.774C>G	ENSP00000490709.1:p.Ala258=
ENST00000635958.1:n.885C>G
ENST00000635973.1:c.525C>G	ENSP00000490363.1:p.Ala175=
ENST00000636017.1:c.*298C>G	ENSP00000490538.1:n.*298C>G
ENST00000636078.1:n.816C>G
ENST00000636147.2:c.774C>G MANE Select	ENSP00000490105.1:p.Ala258=
ENST00000636172.1:c.*298C>G	ENSP00000490505.1:n.*298C>G
ENST00000636228.1:c.468C>G	ENSP00000489627.1:p.Ala156=
ENST00000636351.1:n.494C>G
ENST00000636503.1:c.774C>G	ENSP00000489824.1:p.Ala258=
ENST00000636685.1:n.281C>G
ENST00000636766.1:c.774C>G	ENSP00000489841.1:p.Ala258=
ENST00000636839.1:n.926C>G
ENST00000636853.1:n.1689C>G
ENST00000636866.1:c.774C>G	ENSP00000490880.1:p.Ala258=
ENST00000636907.1:n.925C>G
ENST00000636977.1:n.1842C>G
ENST00000637050.1:n.861C>G
ENST00000637100.1:c.774C>G	ENSP00000490394.1:p.Ala258=
ENST00000637107.1:c.*298C>G	ENSP00000490248.1:n.*298C>G
ENST00000637184.1:c.774C>G	ENSP00000489952.1:p.Ala258=
ENST00000637299.1:c.*583C>G	ENSP00000489823.1:n.*583C>G
ENST00000637376.1:c.774C>G	ENSP00000490758.1:p.Ala258=
ENST00000637578.1:c.*298C>G	ENSP00000490206.1:n.*298C>G
ENST00000637699.1:c.557C>G	ENSP00000490049.1:n.557C>G
ENST00000637745.1:c.113C>G
ENST00000637871.1:c.*298C>G	ENSP00000490670.1:n.*298C>G
ENST00000333496.13:c.702C>G	ENSP00000329171.9:p.Ala234=
ENST00000355477.9:c.*11C>G	ENSP00000347660.6:n.*11C>G
ENST00000357806.11:c.477C>G	ENSP00000350457.7:p.Ala159=
ENST00000357857.13:c.612C>G	ENSP00000350523.9:p.Ala204=
ENST00000359984.11:c.468C>G	ENSP00000353073.8:p.Ala156=
ENST00000360019.6:c.774C>G	ENSP00000353116.2:p.Ala258=
ENST00000395653.8:c.474C>G	ENSP00000379014.4:p.Ala158=
ENST00000561689.5:n.615C>G
ENST00000563874.5:n.2128C>G
ENST00000564574.5:n.822C>G
ENST00000565047.1:n.368C>G
ENST00000565140.5:c.557C>G	ENSP00000455342.1:n.557C>G
ENST00000565316.5:c.774C>G	ENSP00000456117.1:p.Ala258=
ENST00000565688.5:c.525C>G	ENSP00000456122.1:p.Ala175=
ENST00000565778.5:c.405C>G	ENSP00000458015.1:p.Ala135=
ENST00000566057.5:c.388C>G	ENSP00000456693.1:n.388C>G
ENST00000566083.5:n.1005C>G
ENST00000566824.5:n.823C>G
ENST00000567495.5:c.*11C>G	ENSP00000456013.1:n.*11C>G
ENST00000567963.5:c.774C>G	ENSP00000455387.1:p.Ala258=
ENST00000568076.5:n.557C>G
ENST00000568224.4:c.540C>G	ENSP00000454253.1:p.Ala180=
ENST00000568422.5:c.*11C>G	ENSP00000455549.1:n.*11C>G
ENST00000568452.5:n.774C>G
ENST00000568472.5:n.254C>G
ENST00000568497.5:c.*70C>G	ENSP00000456414.1:n.*70C>G
ENST00000568558.5:c.315C>G	ENSP00000455603.1:p.Ala105=
ENST00000569030.5:c.461-1350C>G	ENSP00000454680.1:n.461-1350C>G
ENST00000569430.5:c.774C>G	ENSP00000454229.1:p.Ala258=
ENST00000628023.2:c.*70C>G	ENSP00000486178.1:n.*70C>G
ENST00000631023.2:c.774C>G	ENSP00000486616.1:p.Ala258=
NM_000086.2:c.774C>G , LRG_689t1:c.774C>G	NP_000077.1:p.Ala258=
NM_001042432.1:c.774C>G , LRG_689t2:c.774C>G	NP_001035897.1:p.Ala258=
NM_001286104.1:c.702C>G	NP_001273033.1:p.Ala234=
NM_001286105.1:c.474C>G	NP_001273034.1:p.Ala158=
NM_001286109.1:c.540C>G	NP_001273038.1:p.Ala180=
NM_001286110.1:c.612C>G	NP_001273039.1:p.Ala204=
NM_001042432.2:c.774C>G MANE Select	NP_001035897.1:p.Ala258=
NM_001286104.2:c.702C>G	NP_001273033.1:p.Ala234=
NM_001286105.2:c.474C>G	NP_001273034.1:p.Ala158=
NM_001286109.2:c.540C>G	NP_001273038.1:p.Ala180=
NM_001286110.2:c.612C>G	NP_001273039.1:p.Ala204=