Canonical Allele Identifier: CA392973269

Gene: CLN6

Linked Data

• gnomAD v4: 15-68211656-G-T
• MyVariant Identifiers: chr15:g.68503994G>T (hg19) ; chr15:g.68211656G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211656G>T , CM000677.2:g.68211656G>T	GRCh38
NC_000015.9:g.68503994G>T , CM000677.1:g.68503994G>T	GRCh37
NC_000015.8:g.66291048G>T	NCBI36
NG_008764.2:g.50556C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.486+19C>A MANE Select	ENSP00000249806.5:n.486+19C>A
ENST00000562767.2:c.84-14028C>A	ENSP00000456336.1:n.84-14028C>A
ENST00000563917.2:n.328+19C>A
ENST00000565471.6:c.84-1897C>A	ENSP00000457384.1:n.84-1897C>A
ENST00000635747.1:c.*389+19C>A	ENSP00000490627.1:n.*389+19C>A
ENST00000636212.1:c.*56C>A	ENSP00000489851.1:n.*56C>A
ENST00000636314.1:c.183-338C>A	ENSP00000490295.1:n.183-338C>A
ENST00000636674.1:n.1488C>A
ENST00000636964.1:n.1677C>A
ENST00000637054.1:c.198+6880C>A	ENSP00000490807.1:n.198+6880C>A
ENST00000637223.1:c.*201-338C>A	ENSP00000490010.1:n.*201-338C>A
ENST00000637329.1:c.455+19C>A
ENST00000637450.1:c.*140+19C>A	ENSP00000490204.1:n.*140+19C>A
ENST00000637494.1:c.199-338C>A	ENSP00000490057.1:n.199-338C>A
ENST00000637667.1:c.387+19C>A	ENSP00000489843.1:n.387+19C>A
ENST00000637823.1:c.224-13C>A
ENST00000637888.1:c.198+6880C>A	ENSP00000490546.1:n.198+6880C>A
ENST00000638076.1:c.505C>A	ENSP00000490373.1:p.Pro169Thr
ENST00000638144.1:n.130-338C>A
ENST00000646164.1:c.38+6880C>A
ENST00000249806.9:c.486+19C>A	ENSP00000249806.5:n.486+19C>A
ENST00000538696.5:c.582+19C>A	ENSP00000445770.1:n.582+19C>A
ENST00000562767.1:c.84-14028C>A	ENSP00000456336.1:n.84-14028C>A
ENST00000563917.1:n.286C>A
ENST00000564752.1:c.505C>A	ENSP00000457822.1:p.Pro169Thr
ENST00000565471.5:c.84-1897C>A	ENSP00000457384.1:n.84-1897C>A
ENST00000566347.5:c.298-338C>A	ENSP00000457783.1:n.298-338C>A
ENST00000567060.5:c.298-1936C>A	ENSP00000454818.1:n.298-1936C>A
NM_017882.2:c.486+19C>A	NP_060352.1:n.486+19C>A
XR_931861.1:n.608C>A
NM_017882.3:c.486+19C>A MANE Select	NP_060352.1:n.486+19C>A