Canonical Allele Identifier: CA2184878593
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68218633G= , CM000677.2:g.68218633G= GRCh38
NC_000015.9:g.68510971G= , CM000677.1:g.68510971G= GRCh37
NC_000015.8:g.66298025G= NCBI36
NG_008764.2:g.43579C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.101C= MANE Select ENSP00000249806.5:p.Ala34=
ENST00000562767.2:c.83+10869C= ENSP00000456336.1:n.83+10869C=
ENST00000563917.2:n.41-4245C=
ENST00000565471.6:c.84-8874C= ENSP00000457384.1:n.84-8874C=
ENST00000569336.2:n.10C=
ENST00000635747.1:c.*4C= ENSP00000490627.1:n.*4C=
ENST00000636020.1:n.233C=
ENST00000636212.1:c.101C= ENSP00000489851.1:p.Ala34=
ENST00000636314.1:c.84-4245C= ENSP00000490295.1:n.84-4245C=
ENST00000636876.1:c.*121C= ENSP00000489950.1:n.*121C=
ENST00000637054.1:c.101C= ENSP00000490807.1:p.Ala34=
ENST00000637223.1:c.*4C= ENSP00000490010.1:n.*4C=
ENST00000637329.1:c.12C=
ENST00000637450.1:c.84-4245C= ENSP00000490204.1:n.84-4245C=
ENST00000637494.1:c.101C= ENSP00000490057.1:p.Ala34=
ENST00000637667.1:c.101C= ENSP00000489843.1:p.Ala34=
ENST00000637823.1:c.27C=
ENST00000637888.1:c.101C= ENSP00000490546.1:p.Ala34=
ENST00000638076.1:c.101C= ENSP00000490373.1:p.Ala34=
ENST00000638144.1:n.31-4245C=
ENST00000249806.9:c.101C= ENSP00000249806.5:p.Ala34=
ENST00000538696.5:c.197C= ENSP00000445770.1:p.Ala66=
ENST00000562767.1:c.83+10869C= ENSP00000456336.1:n.83+10869C=
ENST00000564752.1:c.101C= ENSP00000457822.1:p.Ala34=
ENST00000564846.1:n.533C=
ENST00000565471.5:c.84-8874C= ENSP00000457384.1:n.84-8874C=
ENST00000566347.5:c.101C= ENSP00000457783.1:p.Ala34=
ENST00000567060.5:c.101C= ENSP00000454818.1:p.Ala34=
ENST00000569336.1:n.187C=
NM_017882.2:c.101C= NP_060352.1:p.Ala34=
XR_931861.1:n.204C=
NM_017882.3:c.101C= MANE Select NP_060352.1:p.Ala34=