Canonical Allele Identifier: CA2184875133
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68214340C= , CM000677.2:g.68214340C= GRCh38
NC_000015.9:g.68506678C= , CM000677.1:g.68506678C= GRCh37
NC_000015.8:g.66293732C= NCBI36
NG_008764.2:g.47872G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.247G= MANE Select ENSP00000249806.5:p.Asp83=
ENST00000562767.2:c.83+15162G= ENSP00000456336.1:n.83+15162G=
ENST00000563917.2:n.89G=
ENST00000565471.6:c.84-4581G= ENSP00000457384.1:n.84-4581G=
ENST00000635747.1:c.*150G= ENSP00000490627.1:n.*150G=
ENST00000635754.1:n.1269G=
ENST00000636020.1:n.379G=
ENST00000636212.1:c.247G= ENSP00000489851.1:p.Asp83=
ENST00000636314.1:c.132G= ENSP00000490295.1:p.Gly44=
ENST00000637054.1:c.198+4196G= ENSP00000490807.1:n.198+4196G=
ENST00000637223.1:c.*150G= ENSP00000490010.1:n.*150G=
ENST00000637329.1:c.158G=
ENST00000637450.1:c.132G= ENSP00000490204.1:p.Gly44=
ENST00000637494.1:c.199-3022G= ENSP00000490057.1:n.199-3022G=
ENST00000637667.1:c.199-2477G= ENSP00000489843.1:n.199-2477G=
ENST00000637823.1:c.173G=
ENST00000637888.1:c.198+4196G= ENSP00000490546.1:n.198+4196G=
ENST00000638076.1:c.247G= ENSP00000490373.1:p.Asp83=
ENST00000638144.1:n.79G=
ENST00000646164.1:c.38+4196G=
ENST00000249806.9:c.247G= ENSP00000249806.5:p.Asp83=
ENST00000538696.5:c.343G= ENSP00000445770.1:p.Asp115=
ENST00000562767.1:c.83+15162G= ENSP00000456336.1:n.83+15162G=
ENST00000563917.1:n.28G=
ENST00000564752.1:c.247G= ENSP00000457822.1:p.Asp83=
ENST00000564846.1:n.679G=
ENST00000565471.5:c.84-4581G= ENSP00000457384.1:n.84-4581G=
ENST00000566347.5:c.247G= ENSP00000457783.1:p.Asp83=
ENST00000567060.5:c.247G= ENSP00000454818.1:p.Asp83=
NM_017882.2:c.247G= NP_060352.1:p.Asp83=
XR_931861.1:n.350G=
NM_017882.3:c.247G= MANE Select NP_060352.1:p.Asp83=