Canonical Allele Identifier: CA2184872477

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211709T= , CM000677.2:g.68211709T=	GRCh38
NC_000015.9:g.68504047T= , CM000677.1:g.68504047T=	GRCh37
NC_000015.8:g.66291101T=	NCBI36
NG_008764.2:g.50503A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.452A= MANE Select	ENSP00000249806.5:p.Asn151=
ENST00000562767.2:c.84-14081A=	ENSP00000456336.1:n.84-14081A=
ENST00000563917.2:n.294A=
ENST00000565471.6:c.84-1950A=	ENSP00000457384.1:n.84-1950A=
ENST00000635747.1:c.*355A=	ENSP00000490627.1:n.*355A=
ENST00000636212.1:c.*3A=	ENSP00000489851.1:n.*3A=
ENST00000636314.1:c.183-391A=	ENSP00000490295.1:n.183-391A=
ENST00000636674.1:n.1435A=
ENST00000636964.1:n.1624A=
ENST00000637054.1:c.198+6827A=	ENSP00000490807.1:n.198+6827A=
ENST00000637223.1:c.*201-391A=	ENSP00000490010.1:n.*201-391A=
ENST00000637329.1:c.421A=
ENST00000637450.1:c.*106A=	ENSP00000490204.1:n.*106A=
ENST00000637494.1:c.199-391A=	ENSP00000490057.1:n.199-391A=
ENST00000637667.1:c.353A=	ENSP00000489843.1:p.Asn118=
ENST00000637823.1:c.224-66A=
ENST00000637888.1:c.198+6827A=	ENSP00000490546.1:n.198+6827A=
ENST00000638076.1:c.452A=	ENSP00000490373.1:p.Asn151=
ENST00000638144.1:n.130-391A=
ENST00000646164.1:c.38+6827A=
ENST00000249806.9:c.452A=	ENSP00000249806.5:p.Asn151=
ENST00000538696.5:c.548A=	ENSP00000445770.1:p.Asn183=
ENST00000562767.1:c.84-14081A=	ENSP00000456336.1:n.84-14081A=
ENST00000563917.1:n.233A=
ENST00000564752.1:c.452A=	ENSP00000457822.1:p.Asn151=
ENST00000565471.5:c.84-1950A=	ENSP00000457384.1:n.84-1950A=
ENST00000566347.5:c.298-391A=	ENSP00000457783.1:n.298-391A=
ENST00000567060.5:c.298-1989A=	ENSP00000454818.1:n.298-1989A=
NM_017882.2:c.452A=	NP_060352.1:p.Asn151=
XR_931861.1:n.555A=
NM_017882.3:c.452A= MANE Select	NP_060352.1:p.Asn151=