Canonical Allele Identifier: CA392975868

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68510963C>T (hg19) ; chr15:g.68218625C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68218625C>T , CM000677.2:g.68218625C>T	GRCh38
NC_000015.9:g.68510963C>T , CM000677.1:g.68510963C>T	GRCh37
NC_000015.8:g.66298017C>T	NCBI36
NG_008764.2:g.43587G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.109G>A MANE Select	ENSP00000249806.5:p.Ala37Thr
ENST00000562767.2:c.83+10877G>A	ENSP00000456336.1:n.83+10877G>A
ENST00000563917.2:n.41-4237G>A
ENST00000565471.6:c.84-8866G>A	ENSP00000457384.1:n.84-8866G>A
ENST00000569336.2:n.18G>A
ENST00000635747.1:c.*12G>A	ENSP00000490627.1:n.*12G>A
ENST00000636020.1:n.241G>A
ENST00000636212.1:c.109G>A	ENSP00000489851.1:p.Ala37Thr
ENST00000636314.1:c.84-4237G>A	ENSP00000490295.1:n.84-4237G>A
ENST00000636876.1:c.*129G>A	ENSP00000489950.1:n.*129G>A
ENST00000637054.1:c.109G>A	ENSP00000490807.1:p.Ala37Thr
ENST00000637223.1:c.*12G>A	ENSP00000490010.1:n.*12G>A
ENST00000637329.1:c.20G>A
ENST00000637450.1:c.84-4237G>A	ENSP00000490204.1:n.84-4237G>A
ENST00000637494.1:c.109G>A	ENSP00000490057.1:p.Ala37Thr
ENST00000637667.1:c.109G>A	ENSP00000489843.1:p.Ala37Thr
ENST00000637823.1:c.35G>A
ENST00000637888.1:c.109G>A	ENSP00000490546.1:p.Ala37Thr
ENST00000638076.1:c.109G>A	ENSP00000490373.1:p.Ala37Thr
ENST00000638144.1:n.31-4237G>A
ENST00000249806.9:c.109G>A	ENSP00000249806.5:p.Ala37Thr
ENST00000538696.5:c.205G>A	ENSP00000445770.1:p.Ala69Thr
ENST00000562767.1:c.83+10877G>A	ENSP00000456336.1:n.83+10877G>A
ENST00000564752.1:c.109G>A	ENSP00000457822.1:p.Ala37Thr
ENST00000564846.1:n.541G>A
ENST00000565471.5:c.84-8866G>A	ENSP00000457384.1:n.84-8866G>A
ENST00000566347.5:c.109G>A	ENSP00000457783.1:p.Ala37Thr
ENST00000567060.5:c.109G>A	ENSP00000454818.1:p.Ala37Thr
ENST00000569336.1:n.195G>A
NM_017882.2:c.109G>A	NP_060352.1:p.Ala37Thr
XR_931861.1:n.212G>A
NM_017882.3:c.109G>A MANE Select	NP_060352.1:p.Ala37Thr