Canonical Allele Identifier: CA2184884607
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68229596A= , CM000677.2:g.68229596A= GRCh38
NC_000015.9:g.68521934A= , CM000677.1:g.68521934A= GRCh37
NC_000015.8:g.66308988A= NCBI36
NG_008764.2:g.32616T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.-12T= MANE Select ENSP00000249806.5:n.-12T=
ENST00000562767.2:c.-12T= ENSP00000456336.1:n.-12T=
ENST00000563917.2:n.41-15208T=
ENST00000565471.6:c.-12T= ENSP00000457384.1:n.-12T=
ENST00000635747.1:c.173-10946T= ENSP00000490627.1:n.173-10946T=
ENST00000636020.1:n.121T=
ENST00000636212.1:c.-12T= ENSP00000489851.1:n.-12T=
ENST00000636314.1:c.-12T= ENSP00000490295.1:n.-12T=
ENST00000636876.1:c.*104-10946T= ENSP00000489950.1:n.*104-10946T=
ENST00000637054.1:c.-12T= ENSP00000490807.1:n.-12T=
ENST00000637223.1:c.173-10946T= ENSP00000490010.1:n.173-10946T=
ENST00000637450.1:c.-12T= ENSP00000490204.1:n.-12T=
ENST00000637494.1:c.-12T= ENSP00000490057.1:n.-12T=
ENST00000637667.1:c.-12T= ENSP00000489843.1:n.-12T=
ENST00000637888.1:c.-12T= ENSP00000490546.1:n.-12T=
ENST00000638076.1:c.-12T= ENSP00000490373.1:n.-12T=
ENST00000638144.1:n.31-15208T=
ENST00000249806.9:c.-12T= ENSP00000249806.5:n.-12T=
ENST00000538696.5:c.180-10946T= ENSP00000445770.1:n.180-10946T=
ENST00000562767.1:c.-12T= ENSP00000456336.1:n.-12T=
ENST00000564752.1:c.-12T= ENSP00000457822.1:n.-12T=
ENST00000564846.1:n.516-10946T=
ENST00000565471.5:c.-12T= ENSP00000457384.1:n.-12T=
ENST00000566347.5:c.-12T= ENSP00000457783.1:n.-12T=
ENST00000567060.5:c.-12T= ENSP00000454818.1:n.-12T=
ENST00000569336.1:n.75T=
NM_017882.2:c.-12T= NP_060352.1:n.-12T=
XR_931861.1:n.92T=
NM_017882.3:c.-12T= MANE Select NP_060352.1:n.-12T=