Canonical Allele Identifier: CA2629165179

Gene: CLN6

Linked Data

• gnomAD v4: 15-68211956-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211956A>G , CM000677.2:g.68211956A>G	GRCh38
NC_000015.9:g.68504294A>G , CM000677.1:g.68504294A>G	GRCh37
NC_000015.8:g.66291348A>G	NCBI36
NG_008764.2:g.50256T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.298-93T>C MANE Select	ENSP00000249806.5:n.298-93T>C
ENST00000562767.2:c.84-14328T>C	ENSP00000456336.1:n.84-14328T>C
ENST00000563917.2:n.140-93T>C
ENST00000565471.6:c.84-2197T>C	ENSP00000457384.1:n.84-2197T>C
ENST00000635747.1:c.*201-93T>C	ENSP00000490627.1:n.*201-93T>C
ENST00000636212.1:c.298-215T>C	ENSP00000489851.1:n.298-215T>C
ENST00000636314.1:c.183-638T>C	ENSP00000490295.1:n.183-638T>C
ENST00000636674.1:n.1188T>C
ENST00000636964.1:n.1377T>C
ENST00000637054.1:c.198+6580T>C	ENSP00000490807.1:n.198+6580T>C
ENST00000637223.1:c.*201-638T>C	ENSP00000490010.1:n.*201-638T>C
ENST00000637329.1:c.209-35T>C
ENST00000637450.1:c.183-93T>C	ENSP00000490204.1:n.183-93T>C
ENST00000637494.1:c.199-638T>C	ENSP00000490057.1:n.199-638T>C
ENST00000637667.1:c.199-93T>C	ENSP00000489843.1:n.199-93T>C
ENST00000637823.1:c.224-313T>C
ENST00000637888.1:c.198+6580T>C	ENSP00000490546.1:n.198+6580T>C
ENST00000638076.1:c.298-93T>C	ENSP00000490373.1:n.298-93T>C
ENST00000638144.1:n.130-638T>C
ENST00000646164.1:c.38+6580T>C
ENST00000249806.9:c.298-93T>C	ENSP00000249806.5:n.298-93T>C
ENST00000538696.5:c.394-93T>C	ENSP00000445770.1:n.394-93T>C
ENST00000562767.1:c.84-14328T>C	ENSP00000456336.1:n.84-14328T>C
ENST00000563917.1:n.79-93T>C
ENST00000564752.1:c.298-93T>C	ENSP00000457822.1:n.298-93T>C
ENST00000565471.5:c.84-2197T>C	ENSP00000457384.1:n.84-2197T>C
ENST00000566347.5:c.298-638T>C	ENSP00000457783.1:n.298-638T>C
ENST00000567060.5:c.298-2236T>C	ENSP00000454818.1:n.298-2236T>C
NM_017882.2:c.298-93T>C	NP_060352.1:n.298-93T>C
XR_931861.1:n.401-93T>C
NM_017882.3:c.298-93T>C MANE Select	NP_060352.1:n.298-93T>C