Canonical Allele Identifier: CA618694533

Gene: CLN6

Linked Data

• dbSNP Id: rs1386318002
• gnomAD v2: 15-68501937-G-T
• gnomAD v4: 15-68209599-G-T
• MyVariant Identifiers: chr15:g.68501937G>T (hg19) ; chr15:g.68209599G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209599G>T , CM000677.2:g.68209599G>T	GRCh38
NC_000015.9:g.68501937G>T , CM000677.1:g.68501937G>T	GRCh37
NC_000015.8:g.66288991G>T	NCBI36
NG_008764.2:g.52613C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.665+38C>A MANE Select	ENSP00000249806.5:n.665+38C>A
ENST00000562767.2:c.84-11971C>A	ENSP00000456336.1:n.84-11971C>A
ENST00000563917.2:n.507+38C>A
ENST00000565471.6:c.206+38C>A	ENSP00000457384.1:n.206+38C>A
ENST00000635747.1:c.*568+38C>A	ENSP00000490627.1:n.*568+38C>A
ENST00000636212.1:c.*335+38C>A	ENSP00000489851.1:n.*335+38C>A
ENST00000636674.1:n.1767+38C>A
ENST00000636964.1:n.2193+38C>A
ENST00000637054.1:c.198+8937C>A	ENSP00000490807.1:n.198+8937C>A
ENST00000637329.1:c.634+38C>A
ENST00000637450.1:c.*319+38C>A	ENSP00000490204.1:n.*319+38C>A
ENST00000637494.1:c.377+38C>A	ENSP00000490057.1:n.377+38C>A
ENST00000637667.1:c.566+38C>A	ENSP00000489843.1:n.566+38C>A
ENST00000637823.1:c.490+38C>A
ENST00000637888.1:c.198+8937C>A	ENSP00000490546.1:n.198+8937C>A
ENST00000638076.1:c.*268+38C>A	ENSP00000490373.1:n.*268+38C>A
ENST00000638144.1:n.308+38C>A
ENST00000646164.1:c.38+8937C>A
ENST00000249806.9:c.665+38C>A	ENSP00000249806.5:n.665+38C>A
ENST00000538696.5:c.761+38C>A	ENSP00000445770.1:n.761+38C>A
ENST00000562767.1:c.84-11971C>A	ENSP00000456336.1:n.84-11971C>A
ENST00000564752.1:c.*49+38C>A	ENSP00000457822.1:n.*49+38C>A
ENST00000565471.5:c.206+38C>A	ENSP00000457384.1:n.206+38C>A
ENST00000566347.5:c.476+38C>A	ENSP00000457783.1:n.476+38C>A
ENST00000567060.5:c.*63+38C>A	ENSP00000454818.1:n.*63+38C>A
NM_017882.2:c.665+38C>A	NP_060352.1:n.665+38C>A
XR_931861.1:n.887+38C>A
NM_017882.3:c.665+38C>A MANE Select	NP_060352.1:n.665+38C>A