Canonical Allele Identifier: CA272384772

Gene: CLN6

Linked Data

• dbSNP Id: rs982110599
• gnomAD v3: 15-68211931-C-T
• gnomAD v4: 15-68211931-C-T
• MyVariant Identifiers: chr15:g.68504269C>T (hg19) ; chr15:g.68211931C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211931C>T , CM000677.2:g.68211931C>T	GRCh38
NC_000015.9:g.68504269C>T , CM000677.1:g.68504269C>T	GRCh37
NC_000015.8:g.66291323C>T	NCBI36
NG_008764.2:g.50281G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.298-68G>A MANE Select	ENSP00000249806.5:n.298-68G>A
ENST00000562767.2:c.84-14303G>A	ENSP00000456336.1:n.84-14303G>A
ENST00000563917.2:n.140-68G>A
ENST00000565471.6:c.84-2172G>A	ENSP00000457384.1:n.84-2172G>A
ENST00000635747.1:c.*201-68G>A	ENSP00000490627.1:n.*201-68G>A
ENST00000636212.1:c.298-190G>A	ENSP00000489851.1:n.298-190G>A
ENST00000636314.1:c.183-613G>A	ENSP00000490295.1:n.183-613G>A
ENST00000636674.1:n.1213G>A
ENST00000636964.1:n.1402G>A
ENST00000637054.1:c.198+6605G>A	ENSP00000490807.1:n.198+6605G>A
ENST00000637223.1:c.*201-613G>A	ENSP00000490010.1:n.*201-613G>A
ENST00000637329.1:c.209-10G>A
ENST00000637450.1:c.183-68G>A	ENSP00000490204.1:n.183-68G>A
ENST00000637494.1:c.199-613G>A	ENSP00000490057.1:n.199-613G>A
ENST00000637667.1:c.199-68G>A	ENSP00000489843.1:n.199-68G>A
ENST00000637823.1:c.224-288G>A
ENST00000637888.1:c.198+6605G>A	ENSP00000490546.1:n.198+6605G>A
ENST00000638076.1:c.298-68G>A	ENSP00000490373.1:n.298-68G>A
ENST00000638144.1:n.130-613G>A
ENST00000646164.1:c.38+6605G>A
ENST00000249806.9:c.298-68G>A	ENSP00000249806.5:n.298-68G>A
ENST00000538696.5:c.394-68G>A	ENSP00000445770.1:n.394-68G>A
ENST00000562767.1:c.84-14303G>A	ENSP00000456336.1:n.84-14303G>A
ENST00000563917.1:n.79-68G>A
ENST00000564752.1:c.298-68G>A	ENSP00000457822.1:n.298-68G>A
ENST00000565471.5:c.84-2172G>A	ENSP00000457384.1:n.84-2172G>A
ENST00000566347.5:c.298-613G>A	ENSP00000457783.1:n.298-613G>A
ENST00000567060.5:c.298-2211G>A	ENSP00000454818.1:n.298-2211G>A
NM_017882.2:c.298-68G>A	NP_060352.1:n.298-68G>A
XR_931861.1:n.401-68G>A
NM_017882.3:c.298-68G>A MANE Select	NP_060352.1:n.298-68G>A