Canonical Allele Identifier: CA2184872538
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211734G= , CM000677.2:g.68211734G= GRCh38
NC_000015.9:g.68504072G= , CM000677.1:g.68504072G= GRCh37
NC_000015.8:g.66291126G= NCBI36
NG_008764.2:g.50478C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.427C= MANE Select ENSP00000249806.5:p.Gln143=
ENST00000562767.2:c.84-14106C= ENSP00000456336.1:n.84-14106C=
ENST00000563917.2:n.269C=
ENST00000565471.6:c.84-1975C= ENSP00000457384.1:n.84-1975C=
ENST00000635747.1:c.*330C= ENSP00000490627.1:n.*330C=
ENST00000636212.1:c.305C= ENSP00000489851.1:p.Pro102=
ENST00000636314.1:c.183-416C= ENSP00000490295.1:n.183-416C=
ENST00000636674.1:n.1410C=
ENST00000636964.1:n.1599C=
ENST00000637054.1:c.198+6802C= ENSP00000490807.1:n.198+6802C=
ENST00000637223.1:c.*201-416C= ENSP00000490010.1:n.*201-416C=
ENST00000637329.1:c.396C=
ENST00000637450.1:c.*81C= ENSP00000490204.1:n.*81C=
ENST00000637494.1:c.199-416C= ENSP00000490057.1:n.199-416C=
ENST00000637667.1:c.328C= ENSP00000489843.1:p.Gln110=
ENST00000637823.1:c.224-91C=
ENST00000637888.1:c.198+6802C= ENSP00000490546.1:n.198+6802C=
ENST00000638076.1:c.427C= ENSP00000490373.1:p.Gln143=
ENST00000638144.1:n.130-416C=
ENST00000646164.1:c.38+6802C=
ENST00000249806.9:c.427C= ENSP00000249806.5:p.Gln143=
ENST00000538696.5:c.523C= ENSP00000445770.1:p.Gln175=
ENST00000562767.1:c.84-14106C= ENSP00000456336.1:n.84-14106C=
ENST00000563917.1:n.208C=
ENST00000564752.1:c.427C= ENSP00000457822.1:p.Gln143=
ENST00000565471.5:c.84-1975C= ENSP00000457384.1:n.84-1975C=
ENST00000566347.5:c.298-416C= ENSP00000457783.1:n.298-416C=
ENST00000567060.5:c.298-2014C= ENSP00000454818.1:n.298-2014C=
NM_017882.2:c.427C= NP_060352.1:p.Gln143=
XR_931861.1:n.530C=
NM_017882.3:c.427C= MANE Select NP_060352.1:p.Gln143=