Canonical Allele Identifier: CA7630601

Gene: CLN6

Linked Data

• dbSNP Id: rs754600522
• ExAC: 15:68504008 C / T
• gnomAD v2: 15-68504008-C-T
• gnomAD v4: 15-68211670-C-T
• MyVariant Identifiers: chr15:g.68504008C>T (hg19) ; chr15:g.68211670C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211670C>T , CM000677.2:g.68211670C>T	GRCh38
NC_000015.9:g.68504008C>T , CM000677.1:g.68504008C>T	GRCh37
NC_000015.8:g.66291062C>T	NCBI36
NG_008764.2:g.50542G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.486+5G>A MANE Select	ENSP00000249806.5:n.486+5G>A
ENST00000562767.2:c.84-14042G>A	ENSP00000456336.1:n.84-14042G>A
ENST00000563917.2:n.328+5G>A
ENST00000565471.6:c.84-1911G>A	ENSP00000457384.1:n.84-1911G>A
ENST00000635747.1:c.*389+5G>A	ENSP00000490627.1:n.*389+5G>A
ENST00000636212.1:c.*42G>A	ENSP00000489851.1:n.*42G>A
ENST00000636314.1:c.183-352G>A	ENSP00000490295.1:n.183-352G>A
ENST00000636674.1:n.1474G>A
ENST00000636964.1:n.1663G>A
ENST00000637054.1:c.198+6866G>A	ENSP00000490807.1:n.198+6866G>A
ENST00000637223.1:c.*201-352G>A	ENSP00000490010.1:n.*201-352G>A
ENST00000637329.1:c.455+5G>A
ENST00000637450.1:c.*140+5G>A	ENSP00000490204.1:n.*140+5G>A
ENST00000637494.1:c.199-352G>A	ENSP00000490057.1:n.199-352G>A
ENST00000637667.1:c.387+5G>A	ENSP00000489843.1:n.387+5G>A
ENST00000637823.1:c.224-27G>A
ENST00000637888.1:c.198+6866G>A	ENSP00000490546.1:n.198+6866G>A
ENST00000638076.1:c.491G>A	ENSP00000490373.1:p.Arg164Lys
ENST00000638144.1:n.130-352G>A
ENST00000646164.1:c.38+6866G>A
ENST00000249806.9:c.486+5G>A	ENSP00000249806.5:n.486+5G>A
ENST00000538696.5:c.582+5G>A	ENSP00000445770.1:n.582+5G>A
ENST00000562767.1:c.84-14042G>A	ENSP00000456336.1:n.84-14042G>A
ENST00000563917.1:n.272G>A
ENST00000564752.1:c.491G>A	ENSP00000457822.1:p.Arg164Lys
ENST00000565471.5:c.84-1911G>A	ENSP00000457384.1:n.84-1911G>A
ENST00000566347.5:c.298-352G>A	ENSP00000457783.1:n.298-352G>A
ENST00000567060.5:c.298-1950G>A	ENSP00000454818.1:n.298-1950G>A
NM_017882.2:c.486+5G>A	NP_060352.1:n.486+5G>A
XR_931861.1:n.594G>A
NM_017882.3:c.486+5G>A MANE Select	NP_060352.1:n.486+5G>A