Canonical Allele Identifier: CA392973298

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504012C>A (hg19) ; chr15:g.68211674C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211674C>A , CM000677.2:g.68211674C>A	GRCh38
NC_000015.9:g.68504012C>A , CM000677.1:g.68504012C>A	GRCh37
NC_000015.8:g.66291066C>A	NCBI36
NG_008764.2:g.50538G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.486+1G>T MANE Select	ENSP00000249806.5:n.486+1G>T
ENST00000562767.2:c.84-14046G>T	ENSP00000456336.1:n.84-14046G>T
ENST00000563917.2:n.328+1G>T
ENST00000565471.6:c.84-1915G>T	ENSP00000457384.1:n.84-1915G>T
ENST00000635747.1:c.*389+1G>T	ENSP00000490627.1:n.*389+1G>T
ENST00000636212.1:c.*38G>T	ENSP00000489851.1:n.*38G>T
ENST00000636314.1:c.183-356G>T	ENSP00000490295.1:n.183-356G>T
ENST00000636674.1:n.1470G>T
ENST00000636964.1:n.1659G>T
ENST00000637054.1:c.198+6862G>T	ENSP00000490807.1:n.198+6862G>T
ENST00000637223.1:c.*201-356G>T	ENSP00000490010.1:n.*201-356G>T
ENST00000637329.1:c.455+1G>T
ENST00000637450.1:c.*140+1G>T	ENSP00000490204.1:n.*140+1G>T
ENST00000637494.1:c.199-356G>T	ENSP00000490057.1:n.199-356G>T
ENST00000637667.1:c.387+1G>T	ENSP00000489843.1:n.387+1G>T
ENST00000637823.1:c.224-31G>T
ENST00000637888.1:c.198+6862G>T	ENSP00000490546.1:n.198+6862G>T
ENST00000638076.1:c.487G>T	ENSP00000490373.1:p.Val163Leu
ENST00000638144.1:n.130-356G>T
ENST00000646164.1:c.38+6862G>T
ENST00000249806.9:c.486+1G>T	ENSP00000249806.5:n.486+1G>T
ENST00000538696.5:c.582+1G>T	ENSP00000445770.1:n.582+1G>T
ENST00000562767.1:c.84-14046G>T	ENSP00000456336.1:n.84-14046G>T
ENST00000563917.1:n.268G>T
ENST00000564752.1:c.487G>T	ENSP00000457822.1:p.Val163Leu
ENST00000565471.5:c.84-1915G>T	ENSP00000457384.1:n.84-1915G>T
ENST00000566347.5:c.298-356G>T	ENSP00000457783.1:n.298-356G>T
ENST00000567060.5:c.298-1954G>T	ENSP00000454818.1:n.298-1954G>T
NM_017882.2:c.486+1G>T	NP_060352.1:n.486+1G>T
XR_931861.1:n.590G>T
NM_017882.3:c.486+1G>T MANE Select	NP_060352.1:n.486+1G>T