Canonical Allele Identifier: CA2184878599
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68218634C= , CM000677.2:g.68218634C= GRCh38
NC_000015.9:g.68510972C= , CM000677.1:g.68510972C= GRCh37
NC_000015.8:g.66298026C= NCBI36
NG_008764.2:g.43578G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.100G= MANE Select ENSP00000249806.5:p.Ala34=
ENST00000562767.2:c.83+10868G= ENSP00000456336.1:n.83+10868G=
ENST00000563917.2:n.41-4246G=
ENST00000565471.6:c.84-8875G= ENSP00000457384.1:n.84-8875G=
ENST00000569336.2:n.9G=
ENST00000635747.1:c.*3G= ENSP00000490627.1:n.*3G=
ENST00000636020.1:n.232G=
ENST00000636212.1:c.100G= ENSP00000489851.1:p.Ala34=
ENST00000636314.1:c.84-4246G= ENSP00000490295.1:n.84-4246G=
ENST00000636876.1:c.*120G= ENSP00000489950.1:n.*120G=
ENST00000637054.1:c.100G= ENSP00000490807.1:p.Ala34=
ENST00000637223.1:c.*3G= ENSP00000490010.1:n.*3G=
ENST00000637329.1:c.11G=
ENST00000637450.1:c.84-4246G= ENSP00000490204.1:n.84-4246G=
ENST00000637494.1:c.100G= ENSP00000490057.1:p.Ala34=
ENST00000637667.1:c.100G= ENSP00000489843.1:p.Ala34=
ENST00000637823.1:c.26G=
ENST00000637888.1:c.100G= ENSP00000490546.1:p.Ala34=
ENST00000638076.1:c.100G= ENSP00000490373.1:p.Ala34=
ENST00000638144.1:n.31-4246G=
ENST00000249806.9:c.100G= ENSP00000249806.5:p.Ala34=
ENST00000538696.5:c.196G= ENSP00000445770.1:p.Ala66=
ENST00000562767.1:c.83+10868G= ENSP00000456336.1:n.83+10868G=
ENST00000564752.1:c.100G= ENSP00000457822.1:p.Ala34=
ENST00000564846.1:n.532G=
ENST00000565471.5:c.84-8875G= ENSP00000457384.1:n.84-8875G=
ENST00000566347.5:c.100G= ENSP00000457783.1:p.Ala34=
ENST00000567060.5:c.100G= ENSP00000454818.1:p.Ala34=
ENST00000569336.1:n.186G=
NM_017882.2:c.100G= NP_060352.1:p.Ala34=
XR_931861.1:n.203G=
NM_017882.3:c.100G= MANE Select NP_060352.1:p.Ala34=