Canonical Allele Identifier: CA2184872283
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211615G= , CM000677.2:g.68211615G= GRCh38
NC_000015.9:g.68503953G= , CM000677.1:g.68503953G= GRCh37
NC_000015.8:g.66291007G= NCBI36
NG_008764.2:g.50597C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.486+60C= MANE Select ENSP00000249806.5:n.486+60C=
ENST00000562767.2:c.84-13987C= ENSP00000456336.1:n.84-13987C=
ENST00000563917.2:n.328+60C=
ENST00000565471.6:c.84-1856C= ENSP00000457384.1:n.84-1856C=
ENST00000635747.1:c.*389+60C= ENSP00000490627.1:n.*389+60C=
ENST00000636212.1:c.*97C= ENSP00000489851.1:n.*97C=
ENST00000636314.1:c.183-297C= ENSP00000490295.1:n.183-297C=
ENST00000636674.1:n.1529C=
ENST00000636964.1:n.1718C=
ENST00000637054.1:c.198+6921C= ENSP00000490807.1:n.198+6921C=
ENST00000637223.1:c.*201-297C= ENSP00000490010.1:n.*201-297C=
ENST00000637329.1:c.455+60C=
ENST00000637450.1:c.*140+60C= ENSP00000490204.1:n.*140+60C=
ENST00000637494.1:c.199-297C= ENSP00000490057.1:n.199-297C=
ENST00000637667.1:c.387+60C= ENSP00000489843.1:n.387+60C=
ENST00000637823.1:c.252C=
ENST00000637888.1:c.198+6921C= ENSP00000490546.1:n.198+6921C=
ENST00000638076.1:c.*30C= ENSP00000490373.1:n.*30C=
ENST00000638144.1:n.130-297C=
ENST00000646164.1:c.38+6921C=
ENST00000249806.9:c.486+60C= ENSP00000249806.5:n.486+60C=
ENST00000538696.5:c.582+60C= ENSP00000445770.1:n.582+60C=
ENST00000562767.1:c.84-13987C= ENSP00000456336.1:n.84-13987C=
ENST00000563917.1:n.327C=
ENST00000564752.1:c.512+34C= ENSP00000457822.1:n.512+34C=
ENST00000565471.5:c.84-1856C= ENSP00000457384.1:n.84-1856C=
ENST00000566347.5:c.298-297C= ENSP00000457783.1:n.298-297C=
ENST00000567060.5:c.298-1895C= ENSP00000454818.1:n.298-1895C=
NM_017882.2:c.486+60C= NP_060352.1:n.486+60C=
XR_931861.1:n.649C=
NM_017882.3:c.486+60C= MANE Select NP_060352.1:n.486+60C=