Canonical Allele Identifier: CA392973619

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504161G>C (hg19) ; chr15:g.68211823G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211823G>C , CM000677.2:g.68211823G>C	GRCh38
NC_000015.9:g.68504161G>C , CM000677.1:g.68504161G>C	GRCh37
NC_000015.8:g.66291215G>C	NCBI36
NG_008764.2:g.50389C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.338C>G MANE Select	ENSP00000249806.5:p.Thr113Arg
ENST00000562767.2:c.84-14195C>G	ENSP00000456336.1:n.84-14195C>G
ENST00000563917.2:n.180C>G
ENST00000565471.6:c.84-2064C>G	ENSP00000457384.1:n.84-2064C>G
ENST00000635747.1:c.*241C>G	ENSP00000490627.1:n.*241C>G
ENST00000636212.1:c.298-82C>G	ENSP00000489851.1:n.298-82C>G
ENST00000636314.1:c.183-505C>G	ENSP00000490295.1:n.183-505C>G
ENST00000636674.1:n.1321C>G
ENST00000636964.1:n.1510C>G
ENST00000637054.1:c.198+6713C>G	ENSP00000490807.1:n.198+6713C>G
ENST00000637223.1:c.*201-505C>G	ENSP00000490010.1:n.*201-505C>G
ENST00000637329.1:c.307C>G
ENST00000637450.1:c.223C>G	ENSP00000490204.1:p.Arg75Gly
ENST00000637494.1:c.199-505C>G	ENSP00000490057.1:n.199-505C>G
ENST00000637667.1:c.239C>G	ENSP00000489843.1:p.Thr80Arg
ENST00000637823.1:c.224-180C>G
ENST00000637888.1:c.198+6713C>G	ENSP00000490546.1:n.198+6713C>G
ENST00000638076.1:c.338C>G	ENSP00000490373.1:p.Thr113Arg
ENST00000638144.1:n.130-505C>G
ENST00000646164.1:c.38+6713C>G
ENST00000249806.9:c.338C>G	ENSP00000249806.5:p.Thr113Arg
ENST00000538696.5:c.434C>G	ENSP00000445770.1:p.Thr145Arg
ENST00000562767.1:c.84-14195C>G	ENSP00000456336.1:n.84-14195C>G
ENST00000563917.1:n.119C>G
ENST00000564752.1:c.338C>G	ENSP00000457822.1:p.Thr113Arg
ENST00000565471.5:c.84-2064C>G	ENSP00000457384.1:n.84-2064C>G
ENST00000566347.5:c.298-505C>G	ENSP00000457783.1:n.298-505C>G
ENST00000567060.5:c.298-2103C>G	ENSP00000454818.1:n.298-2103C>G
NM_017882.2:c.338C>G	NP_060352.1:p.Thr113Arg
XR_931861.1:n.441C>G
NM_017882.3:c.338C>G MANE Select	NP_060352.1:p.Thr113Arg