Canonical Allele Identifier: CA392973585

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504144T>A (hg19) ; chr15:g.68211806T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211806T>A , CM000677.2:g.68211806T>A	GRCh38
NC_000015.9:g.68504144T>A , CM000677.1:g.68504144T>A	GRCh37
NC_000015.8:g.66291198T>A	NCBI36
NG_008764.2:g.50406A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.355A>T MANE Select	ENSP00000249806.5:p.Ile119Phe
ENST00000562767.2:c.84-14178A>T	ENSP00000456336.1:n.84-14178A>T
ENST00000563917.2:n.197A>T
ENST00000565471.6:c.84-2047A>T	ENSP00000457384.1:n.84-2047A>T
ENST00000635747.1:c.*258A>T	ENSP00000490627.1:n.*258A>T
ENST00000636212.1:c.298-65A>T	ENSP00000489851.1:n.298-65A>T
ENST00000636314.1:c.183-488A>T	ENSP00000490295.1:n.183-488A>T
ENST00000636674.1:n.1338A>T
ENST00000636964.1:n.1527A>T
ENST00000637054.1:c.198+6730A>T	ENSP00000490807.1:n.198+6730A>T
ENST00000637223.1:c.*201-488A>T	ENSP00000490010.1:n.*201-488A>T
ENST00000637329.1:c.324A>T
ENST00000637450.1:c.*9A>T	ENSP00000490204.1:n.*9A>T
ENST00000637494.1:c.199-488A>T	ENSP00000490057.1:n.199-488A>T
ENST00000637667.1:c.256A>T	ENSP00000489843.1:p.Ile86Phe
ENST00000637823.1:c.224-163A>T
ENST00000637888.1:c.198+6730A>T	ENSP00000490546.1:n.198+6730A>T
ENST00000638076.1:c.355A>T	ENSP00000490373.1:p.Ile119Phe
ENST00000638144.1:n.130-488A>T
ENST00000646164.1:c.38+6730A>T
ENST00000249806.9:c.355A>T	ENSP00000249806.5:p.Ile119Phe
ENST00000538696.5:c.451A>T	ENSP00000445770.1:p.Ile151Phe
ENST00000562767.1:c.84-14178A>T	ENSP00000456336.1:n.84-14178A>T
ENST00000563917.1:n.136A>T
ENST00000564752.1:c.355A>T	ENSP00000457822.1:p.Ile119Phe
ENST00000565471.5:c.84-2047A>T	ENSP00000457384.1:n.84-2047A>T
ENST00000566347.5:c.298-488A>T	ENSP00000457783.1:n.298-488A>T
ENST00000567060.5:c.298-2086A>T	ENSP00000454818.1:n.298-2086A>T
NM_017882.2:c.355A>T	NP_060352.1:p.Ile119Phe
XR_931861.1:n.458A>T
NM_017882.3:c.355A>T MANE Select	NP_060352.1:p.Ile119Phe