Canonical Allele Identifier: CA2184872699
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211806T= , CM000677.2:g.68211806T= GRCh38
NC_000015.9:g.68504144T= , CM000677.1:g.68504144T= GRCh37
NC_000015.8:g.66291198T= NCBI36
NG_008764.2:g.50406A=

Transcript Alleles

HGVS Amino-acid change
ENST00000249806.11:c.355A= MANE Select ENSP00000249806.5:p.Ile119=
ENST00000562767.2:c.84-14178A= ENSP00000456336.1:n.84-14178A=
ENST00000563917.2:n.197A=
ENST00000565471.6:c.84-2047A= ENSP00000457384.1:n.84-2047A=
ENST00000635747.1:c.*258A= ENSP00000490627.1:n.*258A=
ENST00000636212.1:c.298-65A= ENSP00000489851.1:n.298-65A=
ENST00000636314.1:c.183-488A= ENSP00000490295.1:n.183-488A=
ENST00000636674.1:n.1338A=
ENST00000636964.1:n.1527A=
ENST00000637054.1:c.198+6730A= ENSP00000490807.1:n.198+6730A=
ENST00000637223.1:c.*201-488A= ENSP00000490010.1:n.*201-488A=
ENST00000637329.1:c.324A=
ENST00000637450.1:c.*9A= ENSP00000490204.1:n.*9A=
ENST00000637494.1:c.199-488A= ENSP00000490057.1:n.199-488A=
ENST00000637667.1:c.256A= ENSP00000489843.1:p.Ile86=
ENST00000637823.1:c.224-163A=
ENST00000637888.1:c.198+6730A= ENSP00000490546.1:n.198+6730A=
ENST00000638076.1:c.355A= ENSP00000490373.1:p.Ile119=
ENST00000638144.1:n.130-488A=
ENST00000646164.1:c.38+6730A=
ENST00000249806.9:c.355A= ENSP00000249806.5:p.Ile119=
ENST00000538696.5:c.451A= ENSP00000445770.1:p.Ile151=
ENST00000562767.1:c.84-14178A= ENSP00000456336.1:n.84-14178A=
ENST00000563917.1:n.136A=
ENST00000564752.1:c.355A= ENSP00000457822.1:p.Ile119=
ENST00000565471.5:c.84-2047A= ENSP00000457384.1:n.84-2047A=
ENST00000566347.5:c.298-488A= ENSP00000457783.1:n.298-488A=
ENST00000567060.5:c.298-2086A= ENSP00000454818.1:n.298-2086A=
NM_017882.2:c.355A= NP_060352.1:p.Ile119=
XR_931861.1:n.458A=
NM_017882.3:c.355A= MANE Select NP_060352.1:p.Ile119=