Canonical Allele Identifier: CA2804591379

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68212008C>G , CM000677.2:g.68212008C>G	GRCh38
NC_000015.9:g.68504346C>G , CM000677.1:g.68504346C>G	GRCh37
NC_000015.8:g.66291400C>G	NCBI36
NG_008764.2:g.50204G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.298-145G>C MANE Select	ENSP00000249806.5:n.298-145G>C
ENST00000562767.2:c.84-14380G>C	ENSP00000456336.1:n.84-14380G>C
ENST00000563917.2:n.140-145G>C
ENST00000565471.6:c.84-2249G>C	ENSP00000457384.1:n.84-2249G>C
ENST00000635747.1:c.*201-145G>C	ENSP00000490627.1:n.*201-145G>C
ENST00000636212.1:c.298-267G>C	ENSP00000489851.1:n.298-267G>C
ENST00000636314.1:c.183-690G>C	ENSP00000490295.1:n.183-690G>C
ENST00000636674.1:n.1136G>C
ENST00000636964.1:n.1325G>C
ENST00000637054.1:c.198+6528G>C	ENSP00000490807.1:n.198+6528G>C
ENST00000637223.1:c.*201-690G>C	ENSP00000490010.1:n.*201-690G>C
ENST00000637329.1:c.209-87G>C
ENST00000637450.1:c.183-145G>C	ENSP00000490204.1:n.183-145G>C
ENST00000637494.1:c.199-690G>C	ENSP00000490057.1:n.199-690G>C
ENST00000637667.1:c.199-145G>C	ENSP00000489843.1:n.199-145G>C
ENST00000637823.1:c.224-365G>C
ENST00000637888.1:c.198+6528G>C	ENSP00000490546.1:n.198+6528G>C
ENST00000638076.1:c.298-145G>C	ENSP00000490373.1:n.298-145G>C
ENST00000638144.1:n.130-690G>C
ENST00000646164.1:c.38+6528G>C
ENST00000249806.9:c.298-145G>C	ENSP00000249806.5:n.298-145G>C
ENST00000538696.5:c.394-145G>C	ENSP00000445770.1:n.394-145G>C
ENST00000562767.1:c.84-14380G>C	ENSP00000456336.1:n.84-14380G>C
ENST00000563917.1:n.79-145G>C
ENST00000564752.1:c.298-145G>C	ENSP00000457822.1:n.298-145G>C
ENST00000565471.5:c.84-2249G>C	ENSP00000457384.1:n.84-2249G>C
ENST00000566347.5:c.298-690G>C	ENSP00000457783.1:n.298-690G>C
ENST00000567060.5:c.297+2282G>C	ENSP00000454818.1:n.297+2282G>C
NM_017882.2:c.298-145G>C	NP_060352.1:n.298-145G>C
XR_931861.1:n.401-145G>C
NM_017882.3:c.298-145G>C MANE Select	NP_060352.1:n.298-145G>C