Canonical Allele Identifier: CA2184879502
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68209653T= , CM000677.2:g.68209653T= GRCh38
NC_000015.9:g.68501991T= , CM000677.1:g.68501991T= GRCh37
NC_000015.8:g.66289045T= NCBI36
NG_008764.2:g.52559A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.649A= MANE Select ENSP00000249806.5:p.Ser217=
ENST00000562767.2:c.84-12025A= ENSP00000456336.1:n.84-12025A=
ENST00000563917.2:n.491A=
ENST00000565471.6:c.190A= ENSP00000457384.1:p.Ser64=
ENST00000635747.1:c.*552A= ENSP00000490627.1:n.*552A=
ENST00000636212.1:c.*319A= ENSP00000489851.1:n.*319A=
ENST00000636674.1:n.1751A=
ENST00000636964.1:n.2177A=
ENST00000637054.1:c.198+8883A= ENSP00000490807.1:n.198+8883A=
ENST00000637329.1:c.618A=
ENST00000637450.1:c.*303A= ENSP00000490204.1:n.*303A=
ENST00000637494.1:c.361A= ENSP00000490057.1:p.Ser121=
ENST00000637667.1:c.550A= ENSP00000489843.1:p.Ser184=
ENST00000637823.1:c.474A=
ENST00000637888.1:c.198+8883A= ENSP00000490546.1:n.198+8883A=
ENST00000638076.1:c.*252A= ENSP00000490373.1:n.*252A=
ENST00000638144.1:n.292A=
ENST00000646164.1:c.38+8883A=
ENST00000249806.9:c.649A= ENSP00000249806.5:p.Ser217=
ENST00000538696.5:c.745A= ENSP00000445770.1:p.Ser249=
ENST00000562767.1:c.84-12025A= ENSP00000456336.1:n.84-12025A=
ENST00000563917.1:n.549A=
ENST00000564752.1:c.*33A= ENSP00000457822.1:n.*33A=
ENST00000565471.5:c.190A= ENSP00000457384.1:p.Ser64=
ENST00000566347.5:c.460A= ENSP00000457783.1:p.Ser154=
ENST00000567060.5:c.*47A= ENSP00000454818.1:n.*47A=
NM_017882.2:c.649A= NP_060352.1:p.Ser217=
XR_931861.1:n.871A=
NM_017882.3:c.649A= MANE Select NP_060352.1:p.Ser217=