Canonical Allele Identifier: CA618694698

Gene: CLN6

Linked Data

• dbSNP Id: rs1239012451
• gnomAD v2: 15-68502123-G-C
• gnomAD v4: 15-68209785-G-C
• MyVariant Identifiers: chr15:g.68502123G>C (hg19) ; chr15:g.68209785G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209785G>C , CM000677.2:g.68209785G>C	GRCh38
NC_000015.9:g.68502123G>C , CM000677.1:g.68502123G>C	GRCh37
NC_000015.8:g.66289177G>C	NCBI36
NG_008764.2:g.52427C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.543-26C>G MANE Select	ENSP00000249806.5:n.543-26C>G
ENST00000562767.2:c.84-12157C>G	ENSP00000456336.1:n.84-12157C>G
ENST00000563917.2:n.385-26C>G
ENST00000565471.6:c.84-26C>G	ENSP00000457384.1:n.84-26C>G
ENST00000635747.1:c.*446-26C>G	ENSP00000490627.1:n.*446-26C>G
ENST00000636212.1:c.*213-26C>G	ENSP00000489851.1:n.*213-26C>G
ENST00000636314.1:c.239-26C>G	ENSP00000490295.1:n.239-26C>G
ENST00000636674.1:n.1645-26C>G
ENST00000636964.1:n.2071-26C>G
ENST00000637054.1:c.198+8751C>G	ENSP00000490807.1:n.198+8751C>G
ENST00000637223.1:c.*257-26C>G	ENSP00000490010.1:n.*257-26C>G
ENST00000637329.1:c.512-26C>G
ENST00000637450.1:c.*197-26C>G	ENSP00000490204.1:n.*197-26C>G
ENST00000637494.1:c.255-26C>G	ENSP00000490057.1:n.255-26C>G
ENST00000637667.1:c.444-26C>G	ENSP00000489843.1:n.444-26C>G
ENST00000637823.1:c.368-26C>G
ENST00000637888.1:c.198+8751C>G	ENSP00000490546.1:n.198+8751C>G
ENST00000638076.1:c.*146-26C>G	ENSP00000490373.1:n.*146-26C>G
ENST00000638144.1:n.186-26C>G
ENST00000646164.1:c.38+8751C>G
ENST00000249806.9:c.543-26C>G	ENSP00000249806.5:n.543-26C>G
ENST00000538696.5:c.639-26C>G	ENSP00000445770.1:n.639-26C>G
ENST00000562767.1:c.84-12157C>G	ENSP00000456336.1:n.84-12157C>G
ENST00000563917.1:n.443-26C>G
ENST00000564752.1:c.569-26C>G	ENSP00000457822.1:n.569-26C>G
ENST00000565471.5:c.84-26C>G	ENSP00000457384.1:n.84-26C>G
ENST00000566347.5:c.354-26C>G	ENSP00000457783.1:n.354-26C>G
ENST00000567060.5:c.298-65C>G	ENSP00000454818.1:n.298-65C>G
NM_017882.2:c.543-26C>G	NP_060352.1:n.543-26C>G
XR_931861.1:n.765-26C>G
NM_017882.3:c.543-26C>G MANE Select	NP_060352.1:n.543-26C>G