Canonical Allele Identifier: CA392973661

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504179G>T (hg19) ; chr15:g.68211841G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211841G>T , CM000677.2:g.68211841G>T	GRCh38
NC_000015.9:g.68504179G>T , CM000677.1:g.68504179G>T	GRCh37
NC_000015.8:g.66291233G>T	NCBI36
NG_008764.2:g.50371C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.320C>A MANE Select	ENSP00000249806.5:p.Thr107Asn
ENST00000562767.2:c.84-14213C>A	ENSP00000456336.1:n.84-14213C>A
ENST00000563917.2:n.162C>A
ENST00000565471.6:c.84-2082C>A	ENSP00000457384.1:n.84-2082C>A
ENST00000635747.1:c.*223C>A	ENSP00000490627.1:n.*223C>A
ENST00000636212.1:c.298-100C>A	ENSP00000489851.1:n.298-100C>A
ENST00000636314.1:c.183-523C>A	ENSP00000490295.1:n.183-523C>A
ENST00000636674.1:n.1303C>A
ENST00000636964.1:n.1492C>A
ENST00000637054.1:c.198+6695C>A	ENSP00000490807.1:n.198+6695C>A
ENST00000637223.1:c.*201-523C>A	ENSP00000490010.1:n.*201-523C>A
ENST00000637329.1:c.289C>A
ENST00000637450.1:c.205C>A	ENSP00000490204.1:p.Pro69Thr
ENST00000637494.1:c.199-523C>A	ENSP00000490057.1:n.199-523C>A
ENST00000637667.1:c.221C>A	ENSP00000489843.1:p.Thr74Asn
ENST00000637823.1:c.224-198C>A
ENST00000637888.1:c.198+6695C>A	ENSP00000490546.1:n.198+6695C>A
ENST00000638076.1:c.320C>A	ENSP00000490373.1:p.Thr107Asn
ENST00000638144.1:n.130-523C>A
ENST00000646164.1:c.38+6695C>A
ENST00000249806.9:c.320C>A	ENSP00000249806.5:p.Thr107Asn
ENST00000538696.5:c.416C>A	ENSP00000445770.1:p.Thr139Asn
ENST00000562767.1:c.84-14213C>A	ENSP00000456336.1:n.84-14213C>A
ENST00000563917.1:n.101C>A
ENST00000564752.1:c.320C>A	ENSP00000457822.1:p.Thr107Asn
ENST00000565471.5:c.84-2082C>A	ENSP00000457384.1:n.84-2082C>A
ENST00000566347.5:c.298-523C>A	ENSP00000457783.1:n.298-523C>A
ENST00000567060.5:c.298-2121C>A	ENSP00000454818.1:n.298-2121C>A
NM_017882.2:c.320C>A	NP_060352.1:p.Thr107Asn
XR_931861.1:n.423C>A
NM_017882.3:c.320C>A MANE Select	NP_060352.1:p.Thr107Asn