Canonical Allele Identifier: CA392974350

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68506648T>C (hg19) ; chr15:g.68214310T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68214310T>C , CM000677.2:g.68214310T>C	GRCh38
NC_000015.9:g.68506648T>C , CM000677.1:g.68506648T>C	GRCh37
NC_000015.8:g.66293702T>C	NCBI36
NG_008764.2:g.47902A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.277A>G MANE Select	ENSP00000249806.5:p.Thr93Ala
ENST00000562767.2:c.83+15192A>G	ENSP00000456336.1:n.83+15192A>G
ENST00000563917.2:n.119A>G
ENST00000565471.6:c.84-4551A>G	ENSP00000457384.1:n.84-4551A>G
ENST00000635747.1:c.*180A>G	ENSP00000490627.1:n.*180A>G
ENST00000635754.1:n.1299A>G
ENST00000636020.1:n.409A>G
ENST00000636212.1:c.277A>G	ENSP00000489851.1:p.Thr93Ala
ENST00000636314.1:c.162A>G	ENSP00000490295.1:p.Ser54=
ENST00000637054.1:c.198+4226A>G	ENSP00000490807.1:n.198+4226A>G
ENST00000637223.1:c.*180A>G	ENSP00000490010.1:n.*180A>G
ENST00000637329.1:c.188A>G
ENST00000637450.1:c.162A>G	ENSP00000490204.1:p.Ser54=
ENST00000637494.1:c.199-2992A>G	ENSP00000490057.1:n.199-2992A>G
ENST00000637667.1:c.199-2447A>G	ENSP00000489843.1:n.199-2447A>G
ENST00000637823.1:c.203A>G
ENST00000637888.1:c.198+4226A>G	ENSP00000490546.1:n.198+4226A>G
ENST00000638076.1:c.277A>G	ENSP00000490373.1:p.Thr93Ala
ENST00000638144.1:n.109A>G
ENST00000646164.1:c.38+4226A>G
ENST00000249806.9:c.277A>G	ENSP00000249806.5:p.Thr93Ala
ENST00000538696.5:c.373A>G	ENSP00000445770.1:p.Thr125Ala
ENST00000562767.1:c.83+15192A>G	ENSP00000456336.1:n.83+15192A>G
ENST00000563917.1:n.58A>G
ENST00000564752.1:c.277A>G	ENSP00000457822.1:p.Thr93Ala
ENST00000564846.1:n.709A>G
ENST00000565471.5:c.84-4551A>G	ENSP00000457384.1:n.84-4551A>G
ENST00000566347.5:c.277A>G	ENSP00000457783.1:p.Thr93Ala
ENST00000567060.5:c.277A>G	ENSP00000454818.1:p.Thr93Ala
NM_017882.2:c.277A>G	NP_060352.1:p.Thr93Ala
XR_931861.1:n.380A>G
NM_017882.3:c.277A>G MANE Select	NP_060352.1:p.Thr93Ala