Canonical Allele Identifier: CA658658295

Gene: CLN6

Linked Data

• ClinVar Variation Id: 457975
• ClinVar RCV Id: RCV000555997
• dbSNP Id: rs1401270931
• gnomAD v3: 15-68208415-A-T
• gnomAD v4: 15-68208415-A-T
• MyVariant Identifiers: chr15:g.68500753A>T (hg19) ; chr15:g.68208415A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68208415A>T , CM000677.2:g.68208415A>T	GRCh38
NC_000015.9:g.68500753A>T , CM000677.1:g.68500753A>T	GRCh37
NC_000015.8:g.66287807A>T	NCBI36
NG_008764.2:g.53797T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.666-5T>A MANE Select	ENSP00000249806.5:n.666-5T>A
ENST00000562767.2:c.84-10787T>A	ENSP00000456336.1:n.84-10787T>A
ENST00000563917.2:n.508-5T>A
ENST00000565471.6:c.207-5T>A	ENSP00000457384.1:n.207-5T>A
ENST00000635747.1:c.*569-5T>A	ENSP00000490627.1:n.*569-5T>A
ENST00000636212.1:c.*336-5T>A	ENSP00000489851.1:n.*336-5T>A
ENST00000636674.1:n.1768-5T>A
ENST00000636964.1:n.2194-5T>A
ENST00000637054.1:c.198+10121T>A	ENSP00000490807.1:n.198+10121T>A
ENST00000637329.1:c.635-5T>A
ENST00000637450.1:c.*320-5T>A	ENSP00000490204.1:n.*320-5T>A
ENST00000637494.1:c.378-5T>A	ENSP00000490057.1:n.378-5T>A
ENST00000637667.1:c.567-5T>A	ENSP00000489843.1:n.567-5T>A
ENST00000637823.1:c.491-5T>A
ENST00000637888.1:c.198+10121T>A	ENSP00000490546.1:n.198+10121T>A
ENST00000638076.1:c.*269-5T>A	ENSP00000490373.1:n.*269-5T>A
ENST00000638144.1:n.309-5T>A
ENST00000646164.1:c.39-8734T>A
ENST00000249806.9:c.666-5T>A	ENSP00000249806.5:n.666-5T>A
ENST00000538696.5:c.762-5T>A	ENSP00000445770.1:n.762-5T>A
ENST00000562767.1:c.84-10787T>A	ENSP00000456336.1:n.84-10787T>A
ENST00000564752.1:c.*50-5T>A	ENSP00000457822.1:n.*50-5T>A
ENST00000565471.5:c.207-5T>A	ENSP00000457384.1:n.207-5T>A
ENST00000566347.5:c.477-5T>A	ENSP00000457783.1:n.477-5T>A
ENST00000567060.5:c.*64-5T>A	ENSP00000454818.1:n.*64-5T>A
NM_017882.2:c.666-5T>A	NP_060352.1:n.666-5T>A
XR_931861.1:n.888-5T>A
NM_017882.3:c.666-5T>A MANE Select	NP_060352.1:n.666-5T>A