Canonical Allele Identifier: CA2184879633

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209719C= , CM000677.2:g.68209719C=	GRCh38
NC_000015.9:g.68502057C= , CM000677.1:g.68502057C=	GRCh37
NC_000015.8:g.66289111C=	NCBI36
NG_008764.2:g.52493G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.583G= MANE Select	ENSP00000249806.5:p.Gly195=
ENST00000562767.2:c.84-12091G=	ENSP00000456336.1:n.84-12091G=
ENST00000563917.2:n.425G=
ENST00000565471.6:c.124G=	ENSP00000457384.1:p.Gly42=
ENST00000635747.1:c.*486G=	ENSP00000490627.1:n.*486G=
ENST00000636212.1:c.*253G=	ENSP00000489851.1:n.*253G=
ENST00000636314.1:c.279G=	ENSP00000490295.1:p.Ala93=
ENST00000636674.1:n.1685G=
ENST00000636964.1:n.2111G=
ENST00000637054.1:c.198+8817G=	ENSP00000490807.1:n.198+8817G=
ENST00000637223.1:c.*297G=	ENSP00000490010.1:n.*297G=
ENST00000637329.1:c.552G=
ENST00000637450.1:c.*237G=	ENSP00000490204.1:n.*237G=
ENST00000637494.1:c.295G=	ENSP00000490057.1:p.Gly99=
ENST00000637667.1:c.484G=	ENSP00000489843.1:p.Gly162=
ENST00000637823.1:c.408G=
ENST00000637888.1:c.198+8817G=	ENSP00000490546.1:n.198+8817G=
ENST00000638076.1:c.*186G=	ENSP00000490373.1:n.*186G=
ENST00000638144.1:n.226G=
ENST00000646164.1:c.38+8817G=
ENST00000249806.9:c.583G=	ENSP00000249806.5:p.Gly195=
ENST00000538696.5:c.679G=	ENSP00000445770.1:p.Gly227=
ENST00000562767.1:c.84-12091G=	ENSP00000456336.1:n.84-12091G=
ENST00000563917.1:n.483G=
ENST00000564752.1:c.609G=	ENSP00000457822.1:p.Ala203=
ENST00000565471.5:c.124G=	ENSP00000457384.1:p.Gly42=
ENST00000566347.5:c.394G=	ENSP00000457783.1:p.Gly132=
ENST00000567060.5:c.299G=	ENSP00000454818.1:p.Arg100=
NM_017882.2:c.583G=	NP_060352.1:p.Gly195=
XR_931861.1:n.805G=
NM_017882.3:c.583G= MANE Select	NP_060352.1:p.Gly195=