Canonical Allele Identifier: CA490913105

Gene: CLN6

Linked Data

• COSMIC: COSM5767005
• MyVariant Identifiers: chr15:g.68504172T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211834T>C , CM000677.2:g.68211834T>C	GRCh38
NC_000015.9:g.68504172T>C , CM000677.1:g.68504172T>C	GRCh37
NC_000015.8:g.66291226T>C	NCBI36
NG_008764.2:g.50378A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.327A>G MANE Select	ENSP00000249806.5:p.Pro109=
ENST00000562767.2:c.84-14206A>G	ENSP00000456336.1:n.84-14206A>G
ENST00000563917.2:n.169A>G
ENST00000565471.6:c.84-2075A>G	ENSP00000457384.1:n.84-2075A>G
ENST00000635747.1:c.*230A>G	ENSP00000490627.1:n.*230A>G
ENST00000636212.1:c.298-93A>G	ENSP00000489851.1:n.298-93A>G
ENST00000636314.1:c.183-516A>G	ENSP00000490295.1:n.183-516A>G
ENST00000636674.1:n.1310A>G
ENST00000636964.1:n.1499A>G
ENST00000637054.1:c.198+6702A>G	ENSP00000490807.1:n.198+6702A>G
ENST00000637223.1:c.*201-516A>G	ENSP00000490010.1:n.*201-516A>G
ENST00000637329.1:c.296A>G
ENST00000637450.1:c.212A>G	ENSP00000490204.1:p.His71Arg
ENST00000637494.1:c.199-516A>G	ENSP00000490057.1:n.199-516A>G
ENST00000637667.1:c.228A>G	ENSP00000489843.1:p.Pro76=
ENST00000637823.1:c.224-191A>G
ENST00000637888.1:c.198+6702A>G	ENSP00000490546.1:n.198+6702A>G
ENST00000638076.1:c.327A>G	ENSP00000490373.1:p.Pro109=
ENST00000638144.1:n.130-516A>G
ENST00000646164.1:c.38+6702A>G
ENST00000249806.9:c.327A>G	ENSP00000249806.5:p.Pro109=
ENST00000538696.5:c.423A>G	ENSP00000445770.1:p.Pro141=
ENST00000562767.1:c.84-14206A>G	ENSP00000456336.1:n.84-14206A>G
ENST00000563917.1:n.108A>G
ENST00000564752.1:c.327A>G	ENSP00000457822.1:p.Pro109=
ENST00000565471.5:c.84-2075A>G	ENSP00000457384.1:n.84-2075A>G
ENST00000566347.5:c.298-516A>G	ENSP00000457783.1:n.298-516A>G
ENST00000567060.5:c.298-2114A>G	ENSP00000454818.1:n.298-2114A>G
NM_017882.2:c.327A>G	NP_060352.1:p.Pro109=
XR_931861.1:n.430A>G
NM_017882.3:c.327A>G MANE Select	NP_060352.1:p.Pro109=