Canonical Allele Identifier: CA392973623

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504162T>C (hg19) ; chr15:g.68211824T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211824T>C , CM000677.2:g.68211824T>C	GRCh38
NC_000015.9:g.68504162T>C , CM000677.1:g.68504162T>C	GRCh37
NC_000015.8:g.66291216T>C	NCBI36
NG_008764.2:g.50388A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.337A>G MANE Select	ENSP00000249806.5:p.Thr113Ala
ENST00000562767.2:c.84-14196A>G	ENSP00000456336.1:n.84-14196A>G
ENST00000563917.2:n.179A>G
ENST00000565471.6:c.84-2065A>G	ENSP00000457384.1:n.84-2065A>G
ENST00000635747.1:c.*240A>G	ENSP00000490627.1:n.*240A>G
ENST00000636212.1:c.298-83A>G	ENSP00000489851.1:n.298-83A>G
ENST00000636314.1:c.183-506A>G	ENSP00000490295.1:n.183-506A>G
ENST00000636674.1:n.1320A>G
ENST00000636964.1:n.1509A>G
ENST00000637054.1:c.198+6712A>G	ENSP00000490807.1:n.198+6712A>G
ENST00000637223.1:c.*201-506A>G	ENSP00000490010.1:n.*201-506A>G
ENST00000637329.1:c.306A>G
ENST00000637450.1:c.222A>G	ENSP00000490204.1:p.Ser74=
ENST00000637494.1:c.199-506A>G	ENSP00000490057.1:n.199-506A>G
ENST00000637667.1:c.238A>G	ENSP00000489843.1:p.Thr80Ala
ENST00000637823.1:c.224-181A>G
ENST00000637888.1:c.198+6712A>G	ENSP00000490546.1:n.198+6712A>G
ENST00000638076.1:c.337A>G	ENSP00000490373.1:p.Thr113Ala
ENST00000638144.1:n.130-506A>G
ENST00000646164.1:c.38+6712A>G
ENST00000249806.9:c.337A>G	ENSP00000249806.5:p.Thr113Ala
ENST00000538696.5:c.433A>G	ENSP00000445770.1:p.Thr145Ala
ENST00000562767.1:c.84-14196A>G	ENSP00000456336.1:n.84-14196A>G
ENST00000563917.1:n.118A>G
ENST00000564752.1:c.337A>G	ENSP00000457822.1:p.Thr113Ala
ENST00000565471.5:c.84-2065A>G	ENSP00000457384.1:n.84-2065A>G
ENST00000566347.5:c.298-506A>G	ENSP00000457783.1:n.298-506A>G
ENST00000567060.5:c.298-2104A>G	ENSP00000454818.1:n.298-2104A>G
NM_017882.2:c.337A>G	NP_060352.1:p.Thr113Ala
XR_931861.1:n.440A>G
NM_017882.3:c.337A>G MANE Select	NP_060352.1:p.Thr113Ala