Canonical Allele Identifier: CA2184872679
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211803A= , CM000677.2:g.68211803A= GRCh38
NC_000015.9:g.68504141A= , CM000677.1:g.68504141A= GRCh37
NC_000015.8:g.66291195A= NCBI36
NG_008764.2:g.50409T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.358T= MANE Select ENSP00000249806.5:p.Phe120=
ENST00000562767.2:c.84-14175T= ENSP00000456336.1:n.84-14175T=
ENST00000563917.2:n.200T=
ENST00000565471.6:c.84-2044T= ENSP00000457384.1:n.84-2044T=
ENST00000635747.1:c.*261T= ENSP00000490627.1:n.*261T=
ENST00000636212.1:c.298-62T= ENSP00000489851.1:n.298-62T=
ENST00000636314.1:c.183-485T= ENSP00000490295.1:n.183-485T=
ENST00000636674.1:n.1341T=
ENST00000636964.1:n.1530T=
ENST00000637054.1:c.198+6733T= ENSP00000490807.1:n.198+6733T=
ENST00000637223.1:c.*201-485T= ENSP00000490010.1:n.*201-485T=
ENST00000637329.1:c.327T=
ENST00000637450.1:c.*12T= ENSP00000490204.1:n.*12T=
ENST00000637494.1:c.199-485T= ENSP00000490057.1:n.199-485T=
ENST00000637667.1:c.259T= ENSP00000489843.1:p.Phe87=
ENST00000637823.1:c.224-160T=
ENST00000637888.1:c.198+6733T= ENSP00000490546.1:n.198+6733T=
ENST00000638076.1:c.358T= ENSP00000490373.1:p.Phe120=
ENST00000638144.1:n.130-485T=
ENST00000646164.1:c.38+6733T=
ENST00000249806.9:c.358T= ENSP00000249806.5:p.Phe120=
ENST00000538696.5:c.454T= ENSP00000445770.1:p.Phe152=
ENST00000562767.1:c.84-14175T= ENSP00000456336.1:n.84-14175T=
ENST00000563917.1:n.139T=
ENST00000564752.1:c.358T= ENSP00000457822.1:p.Phe120=
ENST00000565471.5:c.84-2044T= ENSP00000457384.1:n.84-2044T=
ENST00000566347.5:c.298-485T= ENSP00000457783.1:n.298-485T=
ENST00000567060.5:c.298-2083T= ENSP00000454818.1:n.298-2083T=
NM_017882.2:c.358T= NP_060352.1:p.Phe120=
XR_931861.1:n.461T=
NM_017882.3:c.358T= MANE Select NP_060352.1:p.Phe120=