Canonical Allele Identifier: CA272384779

Gene: CLN6

Linked Data

• dbSNP Id: rs1012356268
• gnomAD v3: 15-68211993-G-A
• gnomAD v4: 15-68211993-G-A
• MyVariant Identifiers: chr15:g.68504331G>A (hg19) ; chr15:g.68211993G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211993G>A , CM000677.2:g.68211993G>A	GRCh38
NC_000015.9:g.68504331G>A , CM000677.1:g.68504331G>A	GRCh37
NC_000015.8:g.66291385G>A	NCBI36
NG_008764.2:g.50219C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.298-130C>T MANE Select	ENSP00000249806.5:n.298-130C>T
ENST00000562767.2:c.84-14365C>T	ENSP00000456336.1:n.84-14365C>T
ENST00000563917.2:n.140-130C>T
ENST00000565471.6:c.84-2234C>T	ENSP00000457384.1:n.84-2234C>T
ENST00000635747.1:c.*201-130C>T	ENSP00000490627.1:n.*201-130C>T
ENST00000636212.1:c.298-252C>T	ENSP00000489851.1:n.298-252C>T
ENST00000636314.1:c.183-675C>T	ENSP00000490295.1:n.183-675C>T
ENST00000636674.1:n.1151C>T
ENST00000636964.1:n.1340C>T
ENST00000637054.1:c.198+6543C>T	ENSP00000490807.1:n.198+6543C>T
ENST00000637223.1:c.*201-675C>T	ENSP00000490010.1:n.*201-675C>T
ENST00000637329.1:c.209-72C>T
ENST00000637450.1:c.183-130C>T	ENSP00000490204.1:n.183-130C>T
ENST00000637494.1:c.199-675C>T	ENSP00000490057.1:n.199-675C>T
ENST00000637667.1:c.199-130C>T	ENSP00000489843.1:n.199-130C>T
ENST00000637823.1:c.224-350C>T
ENST00000637888.1:c.198+6543C>T	ENSP00000490546.1:n.198+6543C>T
ENST00000638076.1:c.298-130C>T	ENSP00000490373.1:n.298-130C>T
ENST00000638144.1:n.130-675C>T
ENST00000646164.1:c.38+6543C>T
ENST00000249806.9:c.298-130C>T	ENSP00000249806.5:n.298-130C>T
ENST00000538696.5:c.394-130C>T	ENSP00000445770.1:n.394-130C>T
ENST00000562767.1:c.84-14365C>T	ENSP00000456336.1:n.84-14365C>T
ENST00000563917.1:n.79-130C>T
ENST00000564752.1:c.298-130C>T	ENSP00000457822.1:n.298-130C>T
ENST00000565471.5:c.84-2234C>T	ENSP00000457384.1:n.84-2234C>T
ENST00000566347.5:c.298-675C>T	ENSP00000457783.1:n.298-675C>T
ENST00000567060.5:c.298-2273C>T	ENSP00000454818.1:n.298-2273C>T
NM_017882.2:c.298-130C>T	NP_060352.1:n.298-130C>T
XR_931861.1:n.401-130C>T
NM_017882.3:c.298-130C>T MANE Select	NP_060352.1:n.298-130C>T