Canonical Allele Identifier: CA2184878561
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68218621G= , CM000677.2:g.68218621G= GRCh38
NC_000015.9:g.68510959G= , CM000677.1:g.68510959G= GRCh37
NC_000015.8:g.66298013G= NCBI36
NG_008764.2:g.43591C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.113C= MANE Select ENSP00000249806.5:p.Ala38=
ENST00000562767.2:c.83+10881C= ENSP00000456336.1:n.83+10881C=
ENST00000563917.2:n.41-4233C=
ENST00000565471.6:c.84-8862C= ENSP00000457384.1:n.84-8862C=
ENST00000569336.2:n.22C=
ENST00000635747.1:c.*16C= ENSP00000490627.1:n.*16C=
ENST00000636020.1:n.245C=
ENST00000636212.1:c.113C= ENSP00000489851.1:p.Ala38=
ENST00000636314.1:c.84-4233C= ENSP00000490295.1:n.84-4233C=
ENST00000636876.1:c.*133C= ENSP00000489950.1:n.*133C=
ENST00000637054.1:c.113C= ENSP00000490807.1:p.Ala38=
ENST00000637223.1:c.*16C= ENSP00000490010.1:n.*16C=
ENST00000637329.1:c.24C=
ENST00000637450.1:c.84-4233C= ENSP00000490204.1:n.84-4233C=
ENST00000637494.1:c.113C= ENSP00000490057.1:p.Ala38=
ENST00000637667.1:c.113C= ENSP00000489843.1:p.Ala38=
ENST00000637823.1:c.39C=
ENST00000637888.1:c.113C= ENSP00000490546.1:p.Ala38=
ENST00000638076.1:c.113C= ENSP00000490373.1:p.Ala38=
ENST00000638144.1:n.31-4233C=
ENST00000249806.9:c.113C= ENSP00000249806.5:p.Ala38=
ENST00000538696.5:c.209C= ENSP00000445770.1:p.Ala70=
ENST00000562767.1:c.83+10881C= ENSP00000456336.1:n.83+10881C=
ENST00000564752.1:c.113C= ENSP00000457822.1:p.Ala38=
ENST00000564846.1:n.545C=
ENST00000565471.5:c.84-8862C= ENSP00000457384.1:n.84-8862C=
ENST00000566347.5:c.113C= ENSP00000457783.1:p.Ala38=
ENST00000567060.5:c.113C= ENSP00000454818.1:p.Ala38=
ENST00000569336.1:n.199C=
NM_017882.2:c.113C= NP_060352.1:p.Ala38=
XR_931861.1:n.216C=
NM_017882.3:c.113C= MANE Select NP_060352.1:p.Ala38=