Canonical Allele Identifier: CA2629163533

Gene: CLN6

Linked Data

• gnomAD v4: 15-68218139-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68218139C>A , CM000677.2:g.68218139C>A	GRCh38
NC_000015.9:g.68510477C>A , CM000677.1:g.68510477C>A	GRCh37
NC_000015.8:g.66297531C>A	NCBI36
NG_008764.2:g.44073G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.198+397G>T MANE Select	ENSP00000249806.5:n.198+397G>T
ENST00000562767.2:c.83+11363G>T	ENSP00000456336.1:n.83+11363G>T
ENST00000563917.2:n.41-3751G>T
ENST00000565471.6:c.84-8380G>T	ENSP00000457384.1:n.84-8380G>T
ENST00000569336.2:n.504G>T
ENST00000635747.1:c.*101+397G>T	ENSP00000490627.1:n.*101+397G>T
ENST00000636020.1:n.330+397G>T
ENST00000636212.1:c.198+397G>T	ENSP00000489851.1:n.198+397G>T
ENST00000636314.1:c.84-3751G>T	ENSP00000490295.1:n.84-3751G>T
ENST00000637054.1:c.198+397G>T	ENSP00000490807.1:n.198+397G>T
ENST00000637223.1:c.*101+397G>T	ENSP00000490010.1:n.*101+397G>T
ENST00000637329.1:c.109+397G>T
ENST00000637450.1:c.84-3751G>T	ENSP00000490204.1:n.84-3751G>T
ENST00000637494.1:c.198+397G>T	ENSP00000490057.1:n.198+397G>T
ENST00000637667.1:c.198+397G>T	ENSP00000489843.1:n.198+397G>T
ENST00000637823.1:c.124+397G>T
ENST00000637888.1:c.198+397G>T	ENSP00000490546.1:n.198+397G>T
ENST00000638076.1:c.198+397G>T	ENSP00000490373.1:n.198+397G>T
ENST00000638144.1:n.31-3751G>T
ENST00000646164.1:c.38+397G>T
ENST00000249806.9:c.198+397G>T	ENSP00000249806.5:n.198+397G>T
ENST00000538696.5:c.294+397G>T	ENSP00000445770.1:n.294+397G>T
ENST00000562767.1:c.83+11363G>T	ENSP00000456336.1:n.83+11363G>T
ENST00000564752.1:c.198+397G>T	ENSP00000457822.1:n.198+397G>T
ENST00000564846.1:n.630+397G>T
ENST00000565471.5:c.84-8380G>T	ENSP00000457384.1:n.84-8380G>T
ENST00000566347.5:c.198+397G>T	ENSP00000457783.1:n.198+397G>T
ENST00000567060.5:c.198+397G>T	ENSP00000454818.1:n.198+397G>T
ENST00000569336.1:n.353+328G>T
NM_017882.2:c.198+397G>T	NP_060352.1:n.198+397G>T
XR_931861.1:n.301+397G>T
NM_017882.3:c.198+397G>T MANE Select	NP_060352.1:n.198+397G>T