Canonical Allele Identifier: CA392973246

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68503985A>C (hg19) ; chr15:g.68211647A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211647A>C , CM000677.2:g.68211647A>C	GRCh38
NC_000015.9:g.68503985A>C , CM000677.1:g.68503985A>C	GRCh37
NC_000015.8:g.66291039A>C	NCBI36
NG_008764.2:g.50565T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.486+28T>G MANE Select	ENSP00000249806.5:n.486+28T>G
ENST00000562767.2:c.84-14019T>G	ENSP00000456336.1:n.84-14019T>G
ENST00000563917.2:n.328+28T>G
ENST00000565471.6:c.84-1888T>G	ENSP00000457384.1:n.84-1888T>G
ENST00000635747.1:c.*389+28T>G	ENSP00000490627.1:n.*389+28T>G
ENST00000636212.1:c.*65T>G	ENSP00000489851.1:n.*65T>G
ENST00000636314.1:c.183-329T>G	ENSP00000490295.1:n.183-329T>G
ENST00000636674.1:n.1497T>G
ENST00000636964.1:n.1686T>G
ENST00000637054.1:c.198+6889T>G	ENSP00000490807.1:n.198+6889T>G
ENST00000637223.1:c.*201-329T>G	ENSP00000490010.1:n.*201-329T>G
ENST00000637329.1:c.455+28T>G
ENST00000637450.1:c.*140+28T>G	ENSP00000490204.1:n.*140+28T>G
ENST00000637494.1:c.199-329T>G	ENSP00000490057.1:n.199-329T>G
ENST00000637667.1:c.387+28T>G	ENSP00000489843.1:n.387+28T>G
ENST00000637823.1:c.224-4T>G
ENST00000637888.1:c.198+6889T>G	ENSP00000490546.1:n.198+6889T>G
ENST00000638076.1:c.514T>G	ENSP00000490373.1:p.Ter172Glu
ENST00000638144.1:n.130-329T>G
ENST00000646164.1:c.38+6889T>G
ENST00000249806.9:c.486+28T>G	ENSP00000249806.5:n.486+28T>G
ENST00000538696.5:c.582+28T>G	ENSP00000445770.1:n.582+28T>G
ENST00000562767.1:c.84-14019T>G	ENSP00000456336.1:n.84-14019T>G
ENST00000563917.1:n.295T>G
ENST00000564752.1:c.512+2T>G	ENSP00000457822.1:n.512+2T>G
ENST00000565471.5:c.84-1888T>G	ENSP00000457384.1:n.84-1888T>G
ENST00000566347.5:c.298-329T>G	ENSP00000457783.1:n.298-329T>G
ENST00000567060.5:c.298-1927T>G	ENSP00000454818.1:n.298-1927T>G
NM_017882.2:c.486+28T>G	NP_060352.1:n.486+28T>G
XR_931861.1:n.617T>G
NM_017882.3:c.486+28T>G MANE Select	NP_060352.1:n.486+28T>G