Canonical Allele Identifier: CA2184872440
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211685G= , CM000677.2:g.68211685G= GRCh38
NC_000015.9:g.68504023G= , CM000677.1:g.68504023G= GRCh37
NC_000015.8:g.66291077G= NCBI36
NG_008764.2:g.50527C=

Transcript Alleles

HGVS Amino-acid change
ENST00000249806.11:c.476C= MANE Select ENSP00000249806.5:p.Pro159=
ENST00000562767.2:c.84-14057C= ENSP00000456336.1:n.84-14057C=
ENST00000563917.2:n.318C=
ENST00000565471.6:c.84-1926C= ENSP00000457384.1:n.84-1926C=
ENST00000635747.1:c.*379C= ENSP00000490627.1:n.*379C=
ENST00000636212.1:c.*27C= ENSP00000489851.1:n.*27C=
ENST00000636314.1:c.183-367C= ENSP00000490295.1:n.183-367C=
ENST00000636674.1:n.1459C=
ENST00000636964.1:n.1648C=
ENST00000637054.1:c.198+6851C= ENSP00000490807.1:n.198+6851C=
ENST00000637223.1:c.*201-367C= ENSP00000490010.1:n.*201-367C=
ENST00000637329.1:c.445C=
ENST00000637450.1:c.*130C= ENSP00000490204.1:n.*130C=
ENST00000637494.1:c.199-367C= ENSP00000490057.1:n.199-367C=
ENST00000637667.1:c.377C= ENSP00000489843.1:p.Pro126=
ENST00000637823.1:c.224-42C=
ENST00000637888.1:c.198+6851C= ENSP00000490546.1:n.198+6851C=
ENST00000638076.1:c.476C= ENSP00000490373.1:p.Pro159=
ENST00000638144.1:n.130-367C=
ENST00000646164.1:c.38+6851C=
ENST00000249806.9:c.476C= ENSP00000249806.5:p.Pro159=
ENST00000538696.5:c.572C= ENSP00000445770.1:p.Pro191=
ENST00000562767.1:c.84-14057C= ENSP00000456336.1:n.84-14057C=
ENST00000563917.1:n.257C=
ENST00000564752.1:c.476C= ENSP00000457822.1:p.Pro159=
ENST00000565471.5:c.84-1926C= ENSP00000457384.1:n.84-1926C=
ENST00000566347.5:c.298-367C= ENSP00000457783.1:n.298-367C=
ENST00000567060.5:c.298-1965C= ENSP00000454818.1:n.298-1965C=
NM_017882.2:c.476C= NP_060352.1:p.Pro159=
XR_931861.1:n.579C=
NM_017882.3:c.476C= MANE Select NP_060352.1:p.Pro159=