Canonical Allele Identifier: CA392973639

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504173G>A (hg19) ; chr15:g.68211835G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211835G>A , CM000677.2:g.68211835G>A	GRCh38
NC_000015.9:g.68504173G>A , CM000677.1:g.68504173G>A	GRCh37
NC_000015.8:g.66291227G>A	NCBI36
NG_008764.2:g.50377C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.326C>T MANE Select	ENSP00000249806.5:p.Pro109Leu
ENST00000562767.2:c.84-14207C>T	ENSP00000456336.1:n.84-14207C>T
ENST00000563917.2:n.168C>T
ENST00000565471.6:c.84-2076C>T	ENSP00000457384.1:n.84-2076C>T
ENST00000635747.1:c.*229C>T	ENSP00000490627.1:n.*229C>T
ENST00000636212.1:c.298-94C>T	ENSP00000489851.1:n.298-94C>T
ENST00000636314.1:c.183-517C>T	ENSP00000490295.1:n.183-517C>T
ENST00000636674.1:n.1309C>T
ENST00000636964.1:n.1498C>T
ENST00000637054.1:c.198+6701C>T	ENSP00000490807.1:n.198+6701C>T
ENST00000637223.1:c.*201-517C>T	ENSP00000490010.1:n.*201-517C>T
ENST00000637329.1:c.295C>T
ENST00000637450.1:c.211C>T	ENSP00000490204.1:p.His71Tyr
ENST00000637494.1:c.199-517C>T	ENSP00000490057.1:n.199-517C>T
ENST00000637667.1:c.227C>T	ENSP00000489843.1:p.Pro76Leu
ENST00000637823.1:c.224-192C>T
ENST00000637888.1:c.198+6701C>T	ENSP00000490546.1:n.198+6701C>T
ENST00000638076.1:c.326C>T	ENSP00000490373.1:p.Pro109Leu
ENST00000638144.1:n.130-517C>T
ENST00000646164.1:c.38+6701C>T
ENST00000249806.9:c.326C>T	ENSP00000249806.5:p.Pro109Leu
ENST00000538696.5:c.422C>T	ENSP00000445770.1:p.Pro141Leu
ENST00000562767.1:c.84-14207C>T	ENSP00000456336.1:n.84-14207C>T
ENST00000563917.1:n.107C>T
ENST00000564752.1:c.326C>T	ENSP00000457822.1:p.Pro109Leu
ENST00000565471.5:c.84-2076C>T	ENSP00000457384.1:n.84-2076C>T
ENST00000566347.5:c.298-517C>T	ENSP00000457783.1:n.298-517C>T
ENST00000567060.5:c.298-2115C>T	ENSP00000454818.1:n.298-2115C>T
NM_017882.2:c.326C>T	NP_060352.1:p.Pro109Leu
XR_931861.1:n.429C>T
NM_017882.3:c.326C>T MANE Select	NP_060352.1:p.Pro109Leu