Canonical Allele Identifier: CA2184872281
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211609T= , CM000677.2:g.68211609T= GRCh38
NC_000015.9:g.68503947T= , CM000677.1:g.68503947T= GRCh37
NC_000015.8:g.66291001T= NCBI36
NG_008764.2:g.50603A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.486+66A= MANE Select ENSP00000249806.5:n.486+66A=
ENST00000562767.2:c.84-13981A= ENSP00000456336.1:n.84-13981A=
ENST00000563917.2:n.328+66A=
ENST00000565471.6:c.84-1850A= ENSP00000457384.1:n.84-1850A=
ENST00000635747.1:c.*389+66A= ENSP00000490627.1:n.*389+66A=
ENST00000636212.1:c.*103A= ENSP00000489851.1:n.*103A=
ENST00000636314.1:c.183-291A= ENSP00000490295.1:n.183-291A=
ENST00000636674.1:n.1535A=
ENST00000636964.1:n.1724A=
ENST00000637054.1:c.198+6927A= ENSP00000490807.1:n.198+6927A=
ENST00000637223.1:c.*201-291A= ENSP00000490010.1:n.*201-291A=
ENST00000637329.1:c.455+66A=
ENST00000637450.1:c.*140+66A= ENSP00000490204.1:n.*140+66A=
ENST00000637494.1:c.199-291A= ENSP00000490057.1:n.199-291A=
ENST00000637667.1:c.387+66A= ENSP00000489843.1:n.387+66A=
ENST00000637823.1:c.258A=
ENST00000637888.1:c.198+6927A= ENSP00000490546.1:n.198+6927A=
ENST00000638076.1:c.*36A= ENSP00000490373.1:n.*36A=
ENST00000638144.1:n.130-291A=
ENST00000646164.1:c.38+6927A=
ENST00000249806.9:c.486+66A= ENSP00000249806.5:n.486+66A=
ENST00000538696.5:c.582+66A= ENSP00000445770.1:n.582+66A=
ENST00000562767.1:c.84-13981A= ENSP00000456336.1:n.84-13981A=
ENST00000563917.1:n.333A=
ENST00000564752.1:c.512+40A= ENSP00000457822.1:n.512+40A=
ENST00000565471.5:c.84-1850A= ENSP00000457384.1:n.84-1850A=
ENST00000566347.5:c.298-291A= ENSP00000457783.1:n.298-291A=
ENST00000567060.5:c.298-1889A= ENSP00000454818.1:n.298-1889A=
NM_017882.2:c.486+66A= NP_060352.1:n.486+66A=
XR_931861.1:n.655A=
NM_017882.3:c.486+66A= MANE Select NP_060352.1:n.486+66A=