Canonical Allele Identifier: CA2184872535
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211733T= , CM000677.2:g.68211733T= GRCh38
NC_000015.9:g.68504071T= , CM000677.1:g.68504071T= GRCh37
NC_000015.8:g.66291125T= NCBI36
NG_008764.2:g.50479A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.428A= MANE Select ENSP00000249806.5:p.Gln143=
ENST00000562767.2:c.84-14105A= ENSP00000456336.1:n.84-14105A=
ENST00000563917.2:n.270A=
ENST00000565471.6:c.84-1974A= ENSP00000457384.1:n.84-1974A=
ENST00000635747.1:c.*331A= ENSP00000490627.1:n.*331A=
ENST00000636212.1:c.306A= ENSP00000489851.1:p.Pro102=
ENST00000636314.1:c.183-415A= ENSP00000490295.1:n.183-415A=
ENST00000636674.1:n.1411A=
ENST00000636964.1:n.1600A=
ENST00000637054.1:c.198+6803A= ENSP00000490807.1:n.198+6803A=
ENST00000637223.1:c.*201-415A= ENSP00000490010.1:n.*201-415A=
ENST00000637329.1:c.397A=
ENST00000637450.1:c.*82A= ENSP00000490204.1:n.*82A=
ENST00000637494.1:c.199-415A= ENSP00000490057.1:n.199-415A=
ENST00000637667.1:c.329A= ENSP00000489843.1:p.Gln110=
ENST00000637823.1:c.224-90A=
ENST00000637888.1:c.198+6803A= ENSP00000490546.1:n.198+6803A=
ENST00000638076.1:c.428A= ENSP00000490373.1:p.Gln143=
ENST00000638144.1:n.130-415A=
ENST00000646164.1:c.38+6803A=
ENST00000249806.9:c.428A= ENSP00000249806.5:p.Gln143=
ENST00000538696.5:c.524A= ENSP00000445770.1:p.Gln175=
ENST00000562767.1:c.84-14105A= ENSP00000456336.1:n.84-14105A=
ENST00000563917.1:n.209A=
ENST00000564752.1:c.428A= ENSP00000457822.1:p.Gln143=
ENST00000565471.5:c.84-1974A= ENSP00000457384.1:n.84-1974A=
ENST00000566347.5:c.298-415A= ENSP00000457783.1:n.298-415A=
ENST00000567060.5:c.298-2013A= ENSP00000454818.1:n.298-2013A=
NM_017882.2:c.428A= NP_060352.1:p.Gln143=
XR_931861.1:n.531A=
NM_017882.3:c.428A= MANE Select NP_060352.1:p.Gln143=