Canonical Allele Identifier: CA2184884614
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68229598G= , CM000677.2:g.68229598G= GRCh38
NC_000015.9:g.68521936G= , CM000677.1:g.68521936G= GRCh37
NC_000015.8:g.66308990G= NCBI36
NG_008764.2:g.32614C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.-14C= MANE Select ENSP00000249806.5:n.-14C=
ENST00000562767.2:c.-14C= ENSP00000456336.1:n.-14C=
ENST00000563917.2:n.41-15210C=
ENST00000565471.6:c.-14C= ENSP00000457384.1:n.-14C=
ENST00000635747.1:c.173-10948C= ENSP00000490627.1:n.173-10948C=
ENST00000636020.1:n.119C=
ENST00000636212.1:c.-14C= ENSP00000489851.1:n.-14C=
ENST00000636314.1:c.-14C= ENSP00000490295.1:n.-14C=
ENST00000636876.1:c.*104-10948C= ENSP00000489950.1:n.*104-10948C=
ENST00000637054.1:c.-14C= ENSP00000490807.1:n.-14C=
ENST00000637223.1:c.173-10948C= ENSP00000490010.1:n.173-10948C=
ENST00000637450.1:c.-14C= ENSP00000490204.1:n.-14C=
ENST00000637494.1:c.-14C= ENSP00000490057.1:n.-14C=
ENST00000637667.1:c.-14C= ENSP00000489843.1:n.-14C=
ENST00000637888.1:c.-14C= ENSP00000490546.1:n.-14C=
ENST00000638076.1:c.-14C= ENSP00000490373.1:n.-14C=
ENST00000638144.1:n.31-15210C=
ENST00000249806.9:c.-14C= ENSP00000249806.5:n.-14C=
ENST00000538696.5:c.180-10948C= ENSP00000445770.1:n.180-10948C=
ENST00000562767.1:c.-14C= ENSP00000456336.1:n.-14C=
ENST00000564752.1:c.-14C= ENSP00000457822.1:n.-14C=
ENST00000564846.1:n.516-10948C=
ENST00000565471.5:c.-14C= ENSP00000457384.1:n.-14C=
ENST00000566347.5:c.-14C= ENSP00000457783.1:n.-14C=
ENST00000567060.5:c.-14C= ENSP00000454818.1:n.-14C=
ENST00000569336.1:n.73C=
NM_017882.2:c.-14C= NP_060352.1:n.-14C=
XR_931861.1:n.90C=
NM_017882.3:c.-14C= MANE Select NP_060352.1:n.-14C=