Canonical Allele Identifier: CA2184872633
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68211790G= , CM000677.2:g.68211790G= GRCh38
NC_000015.9:g.68504128G= , CM000677.1:g.68504128G= GRCh37
NC_000015.8:g.66291182G= NCBI36
NG_008764.2:g.50422C=

Transcript Alleles

HGVS Amino-acid change
ENST00000249806.11:c.371C= MANE Select ENSP00000249806.5:p.Ala124=
ENST00000562767.2:c.84-14162C= ENSP00000456336.1:n.84-14162C=
ENST00000563917.2:n.213C=
ENST00000565471.6:c.84-2031C= ENSP00000457384.1:n.84-2031C=
ENST00000635747.1:c.*274C= ENSP00000490627.1:n.*274C=
ENST00000636212.1:c.298-49C= ENSP00000489851.1:n.298-49C=
ENST00000636314.1:c.183-472C= ENSP00000490295.1:n.183-472C=
ENST00000636674.1:n.1354C=
ENST00000636964.1:n.1543C=
ENST00000637054.1:c.198+6746C= ENSP00000490807.1:n.198+6746C=
ENST00000637223.1:c.*201-472C= ENSP00000490010.1:n.*201-472C=
ENST00000637329.1:c.340C=
ENST00000637450.1:c.*25C= ENSP00000490204.1:n.*25C=
ENST00000637494.1:c.199-472C= ENSP00000490057.1:n.199-472C=
ENST00000637667.1:c.272C= ENSP00000489843.1:p.Ala91=
ENST00000637823.1:c.224-147C=
ENST00000637888.1:c.198+6746C= ENSP00000490546.1:n.198+6746C=
ENST00000638076.1:c.371C= ENSP00000490373.1:p.Ala124=
ENST00000638144.1:n.130-472C=
ENST00000646164.1:c.38+6746C=
ENST00000249806.9:c.371C= ENSP00000249806.5:p.Ala124=
ENST00000538696.5:c.467C= ENSP00000445770.1:p.Ala156=
ENST00000562767.1:c.84-14162C= ENSP00000456336.1:n.84-14162C=
ENST00000563917.1:n.152C=
ENST00000564752.1:c.371C= ENSP00000457822.1:p.Ala124=
ENST00000565471.5:c.84-2031C= ENSP00000457384.1:n.84-2031C=
ENST00000566347.5:c.298-472C= ENSP00000457783.1:n.298-472C=
ENST00000567060.5:c.298-2070C= ENSP00000454818.1:n.298-2070C=
NM_017882.2:c.371C= NP_060352.1:p.Ala124=
XR_931861.1:n.474C=
NM_017882.3:c.371C= MANE Select NP_060352.1:p.Ala124=