Canonical Allele Identifier: CA392975710

Gene: CLN6

Linked Data

• ClinVar Variation Id: 2440146
• ClinVar RCV Id: RCV003145046
• MyVariant Identifiers: chr15:g.68510930A>T (hg19) ; chr15:g.68218592A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68218592A>T , CM000677.2:g.68218592A>T	GRCh38
NC_000015.9:g.68510930A>T , CM000677.1:g.68510930A>T	GRCh37
NC_000015.8:g.66297984A>T	NCBI36
NG_008764.2:g.43620T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.142T>A MANE Select	ENSP00000249806.5:p.Trp48Arg
ENST00000562767.2:c.83+10910T>A	ENSP00000456336.1:n.83+10910T>A
ENST00000563917.2:n.41-4204T>A
ENST00000565471.6:c.84-8833T>A	ENSP00000457384.1:n.84-8833T>A
ENST00000569336.2:n.51T>A
ENST00000635747.1:c.*45T>A	ENSP00000490627.1:n.*45T>A
ENST00000636020.1:n.274T>A
ENST00000636212.1:c.142T>A	ENSP00000489851.1:p.Trp48Arg
ENST00000636314.1:c.84-4204T>A	ENSP00000490295.1:n.84-4204T>A
ENST00000636876.1:c.*162T>A	ENSP00000489950.1:n.*162T>A
ENST00000637054.1:c.142T>A	ENSP00000490807.1:p.Trp48Arg
ENST00000637223.1:c.*45T>A	ENSP00000490010.1:n.*45T>A
ENST00000637329.1:c.53T>A
ENST00000637450.1:c.84-4204T>A	ENSP00000490204.1:n.84-4204T>A
ENST00000637494.1:c.142T>A	ENSP00000490057.1:p.Trp48Arg
ENST00000637667.1:c.142T>A	ENSP00000489843.1:p.Trp48Arg
ENST00000637823.1:c.68T>A
ENST00000637888.1:c.142T>A	ENSP00000490546.1:p.Trp48Arg
ENST00000638076.1:c.142T>A	ENSP00000490373.1:p.Trp48Arg
ENST00000638144.1:n.31-4204T>A
ENST00000249806.9:c.142T>A	ENSP00000249806.5:p.Trp48Arg
ENST00000538696.5:c.238T>A	ENSP00000445770.1:p.Trp80Arg
ENST00000562767.1:c.83+10910T>A	ENSP00000456336.1:n.83+10910T>A
ENST00000564752.1:c.142T>A	ENSP00000457822.1:p.Trp48Arg
ENST00000564846.1:n.574T>A
ENST00000565471.5:c.84-8833T>A	ENSP00000457384.1:n.84-8833T>A
ENST00000566347.5:c.142T>A	ENSP00000457783.1:p.Trp48Arg
ENST00000567060.5:c.142T>A	ENSP00000454818.1:p.Trp48Arg
ENST00000569336.1:n.228T>A
NM_017882.2:c.142T>A	NP_060352.1:p.Trp48Arg
XR_931861.1:n.245T>A
NM_017882.3:c.142T>A MANE Select	NP_060352.1:p.Trp48Arg