Canonical Allele Identifier: CA2629164068

Gene: CLN6

Linked Data

• ClinVar Variation Id: 2708462
• ClinVar RCV Id: RCV003534065
• gnomAD v4: 15-68218662-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68218662C>G , CM000677.2:g.68218662C>G	GRCh38
NC_000015.9:g.68511000C>G , CM000677.1:g.68511000C>G	GRCh37
NC_000015.8:g.66298054C>G	NCBI36
NG_008764.2:g.43550G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.84-12G>C MANE Select	ENSP00000249806.5:n.84-12G>C
ENST00000562767.2:c.83+10840G>C	ENSP00000456336.1:n.83+10840G>C
ENST00000563917.2:n.41-4274G>C
ENST00000565471.6:c.84-8903G>C	ENSP00000457384.1:n.84-8903G>C
ENST00000635747.1:c.173-12G>C	ENSP00000490627.1:n.173-12G>C
ENST00000636020.1:n.216-12G>C
ENST00000636212.1:c.84-12G>C	ENSP00000489851.1:n.84-12G>C
ENST00000636314.1:c.84-4274G>C	ENSP00000490295.1:n.84-4274G>C
ENST00000636876.1:c.*104-12G>C	ENSP00000489950.1:n.*104-12G>C
ENST00000637054.1:c.84-12G>C	ENSP00000490807.1:n.84-12G>C
ENST00000637223.1:c.173-12G>C	ENSP00000490010.1:n.173-12G>C
ENST00000637450.1:c.84-4274G>C	ENSP00000490204.1:n.84-4274G>C
ENST00000637494.1:c.84-12G>C	ENSP00000490057.1:n.84-12G>C
ENST00000637667.1:c.84-12G>C	ENSP00000489843.1:n.84-12G>C
ENST00000637823.1:c.10-12G>C
ENST00000637888.1:c.84-12G>C	ENSP00000490546.1:n.84-12G>C
ENST00000638076.1:c.84-12G>C	ENSP00000490373.1:n.84-12G>C
ENST00000638144.1:n.31-4274G>C
ENST00000249806.9:c.84-12G>C	ENSP00000249806.5:n.84-12G>C
ENST00000538696.5:c.180-12G>C	ENSP00000445770.1:n.180-12G>C
ENST00000562767.1:c.83+10840G>C	ENSP00000456336.1:n.83+10840G>C
ENST00000564752.1:c.84-12G>C	ENSP00000457822.1:n.84-12G>C
ENST00000564846.1:n.516-12G>C
ENST00000565471.5:c.84-8903G>C	ENSP00000457384.1:n.84-8903G>C
ENST00000566347.5:c.84-12G>C	ENSP00000457783.1:n.84-12G>C
ENST00000567060.5:c.84-12G>C	ENSP00000454818.1:n.84-12G>C
ENST00000569336.1:n.170-12G>C
NM_017882.2:c.84-12G>C	NP_060352.1:n.84-12G>C
XR_931861.1:n.187-12G>C
NM_017882.3:c.84-12G>C MANE Select	NP_060352.1:n.84-12G>C