Canonical Allele Identifier: CA2581224497

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211624G>C , CM000677.2:g.68211624G>C	GRCh38
NC_000015.9:g.68503962G>C , CM000677.1:g.68503962G>C	GRCh37
NC_000015.8:g.66291016G>C	NCBI36
NG_008764.2:g.50588C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.486+51C>G MANE Select	ENSP00000249806.5:n.486+51C>G
ENST00000562767.2:c.84-13996C>G	ENSP00000456336.1:n.84-13996C>G
ENST00000563917.2:n.328+51C>G
ENST00000565471.6:c.84-1865C>G	ENSP00000457384.1:n.84-1865C>G
ENST00000635747.1:c.*389+51C>G	ENSP00000490627.1:n.*389+51C>G
ENST00000636212.1:c.*88C>G	ENSP00000489851.1:n.*88C>G
ENST00000636314.1:c.183-306C>G	ENSP00000490295.1:n.183-306C>G
ENST00000636674.1:n.1520C>G
ENST00000636964.1:n.1709C>G
ENST00000637054.1:c.198+6912C>G	ENSP00000490807.1:n.198+6912C>G
ENST00000637223.1:c.*201-306C>G	ENSP00000490010.1:n.*201-306C>G
ENST00000637329.1:c.455+51C>G
ENST00000637450.1:c.*140+51C>G	ENSP00000490204.1:n.*140+51C>G
ENST00000637494.1:c.199-306C>G	ENSP00000490057.1:n.199-306C>G
ENST00000637667.1:c.387+51C>G	ENSP00000489843.1:n.387+51C>G
ENST00000637823.1:c.243C>G
ENST00000637888.1:c.198+6912C>G	ENSP00000490546.1:n.198+6912C>G
ENST00000638076.1:c.*21C>G	ENSP00000490373.1:n.*21C>G
ENST00000638144.1:n.130-306C>G
ENST00000646164.1:c.38+6912C>G
ENST00000249806.9:c.486+51C>G	ENSP00000249806.5:n.486+51C>G
ENST00000538696.5:c.582+51C>G	ENSP00000445770.1:n.582+51C>G
ENST00000562767.1:c.84-13996C>G	ENSP00000456336.1:n.84-13996C>G
ENST00000563917.1:n.318C>G
ENST00000564752.1:c.512+25C>G	ENSP00000457822.1:n.512+25C>G
ENST00000565471.5:c.84-1865C>G	ENSP00000457384.1:n.84-1865C>G
ENST00000566347.5:c.298-306C>G	ENSP00000457783.1:n.298-306C>G
ENST00000567060.5:c.298-1904C>G	ENSP00000454818.1:n.298-1904C>G
NM_017882.2:c.486+51C>G	NP_060352.1:n.486+51C>G
XR_931861.1:n.640C>G
NM_017882.3:c.486+51C>G MANE Select	NP_060352.1:n.486+51C>G