Canonical Allele Identifier: CA392972952

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68502054A>T (hg19) ; chr15:g.68209716A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209716A>T , CM000677.2:g.68209716A>T	GRCh38
NC_000015.9:g.68502054A>T , CM000677.1:g.68502054A>T	GRCh37
NC_000015.8:g.66289108A>T	NCBI36
NG_008764.2:g.52496T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.586T>A MANE Select	ENSP00000249806.5:p.Cys196Ser
ENST00000562767.2:c.84-12088T>A	ENSP00000456336.1:n.84-12088T>A
ENST00000563917.2:n.428T>A
ENST00000565471.6:c.127T>A	ENSP00000457384.1:p.Cys43Ser
ENST00000635747.1:c.*489T>A	ENSP00000490627.1:n.*489T>A
ENST00000636212.1:c.*256T>A	ENSP00000489851.1:n.*256T>A
ENST00000636314.1:c.282T>A	ENSP00000490295.1:p.Ala94=
ENST00000636674.1:n.1688T>A
ENST00000636964.1:n.2114T>A
ENST00000637054.1:c.198+8820T>A	ENSP00000490807.1:n.198+8820T>A
ENST00000637223.1:c.*300T>A	ENSP00000490010.1:n.*300T>A
ENST00000637329.1:c.555T>A
ENST00000637450.1:c.*240T>A	ENSP00000490204.1:n.*240T>A
ENST00000637494.1:c.298T>A	ENSP00000490057.1:p.Cys100Ser
ENST00000637667.1:c.487T>A	ENSP00000489843.1:p.Cys163Ser
ENST00000637823.1:c.411T>A
ENST00000637888.1:c.198+8820T>A	ENSP00000490546.1:n.198+8820T>A
ENST00000638076.1:c.*189T>A	ENSP00000490373.1:n.*189T>A
ENST00000638144.1:n.229T>A
ENST00000646164.1:c.38+8820T>A
ENST00000249806.9:c.586T>A	ENSP00000249806.5:p.Cys196Ser
ENST00000538696.5:c.682T>A	ENSP00000445770.1:p.Cys228Ser
ENST00000562767.1:c.84-12088T>A	ENSP00000456336.1:n.84-12088T>A
ENST00000563917.1:n.486T>A
ENST00000564752.1:c.612T>A	ENSP00000457822.1:p.Ala204=
ENST00000565471.5:c.127T>A	ENSP00000457384.1:p.Cys43Ser
ENST00000566347.5:c.397T>A	ENSP00000457783.1:p.Cys133Ser
ENST00000567060.5:c.302T>A	ENSP00000454818.1:p.Leu101Gln
NM_017882.2:c.586T>A	NP_060352.1:p.Cys196Ser
XR_931861.1:n.808T>A
NM_017882.3:c.586T>A MANE Select	NP_060352.1:p.Cys196Ser