Canonical Allele Identifier: CA2184872637
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211791C= , CM000677.2:g.68211791C= GRCh38
NC_000015.9:g.68504129C= , CM000677.1:g.68504129C= GRCh37
NC_000015.8:g.66291183C= NCBI36
NG_008764.2:g.50421G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.370G= MANE Select ENSP00000249806.5:p.Ala124=
ENST00000562767.2:c.84-14163G= ENSP00000456336.1:n.84-14163G=
ENST00000563917.2:n.212G=
ENST00000565471.6:c.84-2032G= ENSP00000457384.1:n.84-2032G=
ENST00000635747.1:c.*273G= ENSP00000490627.1:n.*273G=
ENST00000636212.1:c.298-50G= ENSP00000489851.1:n.298-50G=
ENST00000636314.1:c.183-473G= ENSP00000490295.1:n.183-473G=
ENST00000636674.1:n.1353G=
ENST00000636964.1:n.1542G=
ENST00000637054.1:c.198+6745G= ENSP00000490807.1:n.198+6745G=
ENST00000637223.1:c.*201-473G= ENSP00000490010.1:n.*201-473G=
ENST00000637329.1:c.339G=
ENST00000637450.1:c.*24G= ENSP00000490204.1:n.*24G=
ENST00000637494.1:c.199-473G= ENSP00000490057.1:n.199-473G=
ENST00000637667.1:c.271G= ENSP00000489843.1:p.Ala91=
ENST00000637823.1:c.224-148G=
ENST00000637888.1:c.198+6745G= ENSP00000490546.1:n.198+6745G=
ENST00000638076.1:c.370G= ENSP00000490373.1:p.Ala124=
ENST00000638144.1:n.130-473G=
ENST00000646164.1:c.38+6745G=
ENST00000249806.9:c.370G= ENSP00000249806.5:p.Ala124=
ENST00000538696.5:c.466G= ENSP00000445770.1:p.Ala156=
ENST00000562767.1:c.84-14163G= ENSP00000456336.1:n.84-14163G=
ENST00000563917.1:n.151G=
ENST00000564752.1:c.370G= ENSP00000457822.1:p.Ala124=
ENST00000565471.5:c.84-2032G= ENSP00000457384.1:n.84-2032G=
ENST00000566347.5:c.298-473G= ENSP00000457783.1:n.298-473G=
ENST00000567060.5:c.298-2071G= ENSP00000454818.1:n.298-2071G=
NM_017882.2:c.370G= NP_060352.1:p.Ala124=
XR_931861.1:n.473G=
NM_017882.3:c.370G= MANE Select NP_060352.1:p.Ala124=