Canonical Allele Identifier: CA2184879850

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209859C= , CM000677.2:g.68209859C=	GRCh38
NC_000015.9:g.68502197C= , CM000677.1:g.68502197C=	GRCh37
NC_000015.8:g.66289251C=	NCBI36
NG_008764.2:g.52353G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.543-100G= MANE Select	ENSP00000249806.5:n.543-100G=
ENST00000562767.2:c.84-12231G=	ENSP00000456336.1:n.84-12231G=
ENST00000563917.2:n.385-100G=
ENST00000565471.6:c.84-100G=	ENSP00000457384.1:n.84-100G=
ENST00000635747.1:c.*446-100G=	ENSP00000490627.1:n.*446-100G=
ENST00000636212.1:c.*213-100G=	ENSP00000489851.1:n.*213-100G=
ENST00000636314.1:c.239-100G=	ENSP00000490295.1:n.239-100G=
ENST00000636674.1:n.1645-100G=
ENST00000636964.1:n.2071-100G=
ENST00000637054.1:c.198+8677G=	ENSP00000490807.1:n.198+8677G=
ENST00000637223.1:c.*257-100G=	ENSP00000490010.1:n.*257-100G=
ENST00000637329.1:c.512-100G=
ENST00000637450.1:c.*197-100G=	ENSP00000490204.1:n.*197-100G=
ENST00000637494.1:c.255-100G=	ENSP00000490057.1:n.255-100G=
ENST00000637667.1:c.444-100G=	ENSP00000489843.1:n.444-100G=
ENST00000637823.1:c.368-100G=
ENST00000637888.1:c.198+8677G=	ENSP00000490546.1:n.198+8677G=
ENST00000638076.1:c.*146-100G=	ENSP00000490373.1:n.*146-100G=
ENST00000638144.1:n.186-100G=
ENST00000646164.1:c.38+8677G=
ENST00000249806.9:c.543-100G=	ENSP00000249806.5:n.543-100G=
ENST00000538696.5:c.639-100G=	ENSP00000445770.1:n.639-100G=
ENST00000562767.1:c.84-12231G=	ENSP00000456336.1:n.84-12231G=
ENST00000563917.1:n.443-100G=
ENST00000564752.1:c.569-100G=	ENSP00000457822.1:n.569-100G=
ENST00000565471.5:c.84-100G=	ENSP00000457384.1:n.84-100G=
ENST00000566347.5:c.354-100G=	ENSP00000457783.1:n.354-100G=
ENST00000567060.5:c.298-139G=	ENSP00000454818.1:n.298-139G=
NM_017882.2:c.543-100G=	NP_060352.1:n.543-100G=
XR_931861.1:n.765-100G=
NM_017882.3:c.543-100G= MANE Select	NP_060352.1:n.543-100G=