Canonical Allele Identifier: CA392972910
Gene: CLN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68209700T>C , CM000677.2:g.68209700T>C GRCh38
NC_000015.9:g.68502038T>C , CM000677.1:g.68502038T>C GRCh37
NC_000015.8:g.66289092T>C NCBI36
NG_008764.2:g.52512A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.602A>G MANE Select ENSP00000249806.5:p.Lys201Arg
ENST00000562767.2:c.84-12072A>G ENSP00000456336.1:n.84-12072A>G
ENST00000563917.2:n.444A>G
ENST00000565471.6:c.143A>G ENSP00000457384.1:p.Lys48Arg
ENST00000635747.1:c.*505A>G ENSP00000490627.1:n.*505A>G
ENST00000636212.1:c.*272A>G ENSP00000489851.1:n.*272A>G
ENST00000636314.1:c.298A>G ENSP00000490295.1:p.Lys100Glu
ENST00000636674.1:n.1704A>G
ENST00000636964.1:n.2130A>G
ENST00000637054.1:c.198+8836A>G ENSP00000490807.1:n.198+8836A>G
ENST00000637329.1:c.571A>G
ENST00000637450.1:c.*256A>G ENSP00000490204.1:n.*256A>G
ENST00000637494.1:c.314A>G ENSP00000490057.1:p.Lys105Arg
ENST00000637667.1:c.503A>G ENSP00000489843.1:p.Lys168Arg
ENST00000637823.1:c.427A>G
ENST00000637888.1:c.198+8836A>G ENSP00000490546.1:n.198+8836A>G
ENST00000638076.1:c.*205A>G ENSP00000490373.1:n.*205A>G
ENST00000638144.1:n.245A>G
ENST00000646164.1:c.38+8836A>G
ENST00000249806.9:c.602A>G ENSP00000249806.5:p.Lys201Arg
ENST00000538696.5:c.698A>G ENSP00000445770.1:p.Lys233Arg
ENST00000562767.1:c.84-12072A>G ENSP00000456336.1:n.84-12072A>G
ENST00000563917.1:n.502A>G
ENST00000564752.1:c.628A>G ENSP00000457822.1:p.Lys210Glu
ENST00000565471.5:c.143A>G ENSP00000457384.1:p.Lys48Arg
ENST00000566347.5:c.413A>G ENSP00000457783.1:p.Lys138Arg
ENST00000567060.5:c.318A>G ENSP00000454818.1:p.Ter106=
NM_017882.2:c.602A>G NP_060352.1:p.Lys201Arg
XR_931861.1:n.824A>G
NM_017882.3:c.602A>G MANE Select NP_060352.1:p.Lys201Arg