Canonical Allele Identifier: CA392973289

Gene: CLN6

Linked Data

• gnomAD v4: 15-68211668-G-T
• MyVariant Identifiers: chr15:g.68504006G>T (hg19) ; chr15:g.68211668G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211668G>T , CM000677.2:g.68211668G>T	GRCh38
NC_000015.9:g.68504006G>T , CM000677.1:g.68504006G>T	GRCh37
NC_000015.8:g.66291060G>T	NCBI36
NG_008764.2:g.50544C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.486+7C>A MANE Select	ENSP00000249806.5:n.486+7C>A
ENST00000562767.2:c.84-14040C>A	ENSP00000456336.1:n.84-14040C>A
ENST00000563917.2:n.328+7C>A
ENST00000565471.6:c.84-1909C>A	ENSP00000457384.1:n.84-1909C>A
ENST00000635747.1:c.*389+7C>A	ENSP00000490627.1:n.*389+7C>A
ENST00000636212.1:c.*44C>A	ENSP00000489851.1:n.*44C>A
ENST00000636314.1:c.183-350C>A	ENSP00000490295.1:n.183-350C>A
ENST00000636674.1:n.1476C>A
ENST00000636964.1:n.1665C>A
ENST00000637054.1:c.198+6868C>A	ENSP00000490807.1:n.198+6868C>A
ENST00000637223.1:c.*201-350C>A	ENSP00000490010.1:n.*201-350C>A
ENST00000637329.1:c.455+7C>A
ENST00000637450.1:c.*140+7C>A	ENSP00000490204.1:n.*140+7C>A
ENST00000637494.1:c.199-350C>A	ENSP00000490057.1:n.199-350C>A
ENST00000637667.1:c.387+7C>A	ENSP00000489843.1:n.387+7C>A
ENST00000637823.1:c.224-25C>A
ENST00000637888.1:c.198+6868C>A	ENSP00000490546.1:n.198+6868C>A
ENST00000638076.1:c.493C>A	ENSP00000490373.1:p.Pro165Thr
ENST00000638144.1:n.130-350C>A
ENST00000646164.1:c.38+6868C>A
ENST00000249806.9:c.486+7C>A	ENSP00000249806.5:n.486+7C>A
ENST00000538696.5:c.582+7C>A	ENSP00000445770.1:n.582+7C>A
ENST00000562767.1:c.84-14040C>A	ENSP00000456336.1:n.84-14040C>A
ENST00000563917.1:n.274C>A
ENST00000564752.1:c.493C>A	ENSP00000457822.1:p.Pro165Thr
ENST00000565471.5:c.84-1909C>A	ENSP00000457384.1:n.84-1909C>A
ENST00000566347.5:c.298-350C>A	ENSP00000457783.1:n.298-350C>A
ENST00000567060.5:c.298-1948C>A	ENSP00000454818.1:n.298-1948C>A
NM_017882.2:c.486+7C>A	NP_060352.1:n.486+7C>A
XR_931861.1:n.596C>A
NM_017882.3:c.486+7C>A MANE Select	NP_060352.1:n.486+7C>A