Canonical Allele Identifier: CA2184872618
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211773C= , CM000677.2:g.68211773C= GRCh38
NC_000015.9:g.68504111C= , CM000677.1:g.68504111C= GRCh37
NC_000015.8:g.66291165C= NCBI36
NG_008764.2:g.50439G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.388G= MANE Select ENSP00000249806.5:p.Gly130=
ENST00000562767.2:c.84-14145G= ENSP00000456336.1:n.84-14145G=
ENST00000563917.2:n.230G=
ENST00000565471.6:c.84-2014G= ENSP00000457384.1:n.84-2014G=
ENST00000635747.1:c.*291G= ENSP00000490627.1:n.*291G=
ENST00000636212.1:c.298-32G= ENSP00000489851.1:n.298-32G=
ENST00000636314.1:c.183-455G= ENSP00000490295.1:n.183-455G=
ENST00000636674.1:n.1371G=
ENST00000636964.1:n.1560G=
ENST00000637054.1:c.198+6763G= ENSP00000490807.1:n.198+6763G=
ENST00000637223.1:c.*201-455G= ENSP00000490010.1:n.*201-455G=
ENST00000637329.1:c.357G=
ENST00000637450.1:c.*42G= ENSP00000490204.1:n.*42G=
ENST00000637494.1:c.199-455G= ENSP00000490057.1:n.199-455G=
ENST00000637667.1:c.289G= ENSP00000489843.1:p.Gly97=
ENST00000637823.1:c.224-130G=
ENST00000637888.1:c.198+6763G= ENSP00000490546.1:n.198+6763G=
ENST00000638076.1:c.388G= ENSP00000490373.1:p.Gly130=
ENST00000638144.1:n.130-455G=
ENST00000646164.1:c.38+6763G=
ENST00000249806.9:c.388G= ENSP00000249806.5:p.Gly130=
ENST00000538696.5:c.484G= ENSP00000445770.1:p.Gly162=
ENST00000562767.1:c.84-14145G= ENSP00000456336.1:n.84-14145G=
ENST00000563917.1:n.169G=
ENST00000564752.1:c.388G= ENSP00000457822.1:p.Gly130=
ENST00000565471.5:c.84-2014G= ENSP00000457384.1:n.84-2014G=
ENST00000566347.5:c.298-455G= ENSP00000457783.1:n.298-455G=
ENST00000567060.5:c.298-2053G= ENSP00000454818.1:n.298-2053G=
NM_017882.2:c.388G= NP_060352.1:p.Gly130=
XR_931861.1:n.491G=
NM_017882.3:c.388G= MANE Select NP_060352.1:p.Gly130=