Canonical Allele Identifier: CA2184877794
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68208174G= , CM000677.2:g.68208174G= GRCh38
NC_000015.9:g.68500512G= , CM000677.1:g.68500512G= GRCh37
NC_000015.8:g.66287566G= NCBI36
NG_008764.2:g.54038C=

Transcript Alleles

HGVS Amino-acid change
ENST00000249806.11:c.902C= MANE Select ENSP00000249806.5:p.Ala301=
ENST00000562767.2:c.84-10546C= ENSP00000456336.1:n.84-10546C=
ENST00000565471.6:c.443C= ENSP00000457384.1:p.Ala148=
ENST00000635747.1:c.*805C= ENSP00000490627.1:n.*805C=
ENST00000636212.1:c.*572C= ENSP00000489851.1:n.*572C=
ENST00000636674.1:n.2004C=
ENST00000636964.1:n.2430C=
ENST00000637054.1:c.198+10362C= ENSP00000490807.1:n.198+10362C=
ENST00000637329.1:c.871C=
ENST00000637494.1:c.614C= ENSP00000490057.1:p.Ala205=
ENST00000637888.1:c.198+10362C= ENSP00000490546.1:n.198+10362C=
ENST00000638076.1:c.*505C= ENSP00000490373.1:n.*505C=
ENST00000638144.1:n.545C=
ENST00000646164.1:c.39-8493C=
ENST00000249806.9:c.902C= ENSP00000249806.5:p.Ala301=
ENST00000538696.5:c.998C= ENSP00000445770.1:p.Ala333=
ENST00000562767.1:c.84-10546C= ENSP00000456336.1:n.84-10546C=
ENST00000565471.5:c.443C= ENSP00000457384.1:p.Ala148=
ENST00000566347.5:c.713C= ENSP00000457783.1:p.Ala238=
ENST00000567060.5:c.*300C= ENSP00000454818.1:n.*300C=
NM_017882.2:c.902C= NP_060352.1:p.Ala301=
NM_017882.3:c.902C= MANE Select NP_060352.1:p.Ala301=