Canonical Allele Identifier: CA2629164443

Gene: CLN6

Linked Data

• gnomAD v4: 15-68209762-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209762G>A , CM000677.2:g.68209762G>A	GRCh38
NC_000015.9:g.68502100G>A , CM000677.1:g.68502100G>A	GRCh37
NC_000015.8:g.66289154G>A	NCBI36
NG_008764.2:g.52450C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.543-3C>T MANE Select	ENSP00000249806.5:n.543-3C>T
ENST00000562767.2:c.84-12134C>T	ENSP00000456336.1:n.84-12134C>T
ENST00000563917.2:n.385-3C>T
ENST00000565471.6:c.84-3C>T	ENSP00000457384.1:n.84-3C>T
ENST00000635747.1:c.*446-3C>T	ENSP00000490627.1:n.*446-3C>T
ENST00000636212.1:c.*213-3C>T	ENSP00000489851.1:n.*213-3C>T
ENST00000636314.1:c.239-3C>T	ENSP00000490295.1:n.239-3C>T
ENST00000636674.1:n.1645-3C>T
ENST00000636964.1:n.2071-3C>T
ENST00000637054.1:c.198+8774C>T	ENSP00000490807.1:n.198+8774C>T
ENST00000637223.1:c.*257-3C>T	ENSP00000490010.1:n.*257-3C>T
ENST00000637329.1:c.512-3C>T
ENST00000637450.1:c.*197-3C>T	ENSP00000490204.1:n.*197-3C>T
ENST00000637494.1:c.255-3C>T	ENSP00000490057.1:n.255-3C>T
ENST00000637667.1:c.444-3C>T	ENSP00000489843.1:n.444-3C>T
ENST00000637823.1:c.368-3C>T
ENST00000637888.1:c.198+8774C>T	ENSP00000490546.1:n.198+8774C>T
ENST00000638076.1:c.*146-3C>T	ENSP00000490373.1:n.*146-3C>T
ENST00000638144.1:n.186-3C>T
ENST00000646164.1:c.38+8774C>T
ENST00000249806.9:c.543-3C>T	ENSP00000249806.5:n.543-3C>T
ENST00000538696.5:c.639-3C>T	ENSP00000445770.1:n.639-3C>T
ENST00000562767.1:c.84-12134C>T	ENSP00000456336.1:n.84-12134C>T
ENST00000563917.1:n.443-3C>T
ENST00000564752.1:c.569-3C>T	ENSP00000457822.1:n.569-3C>T
ENST00000565471.5:c.84-3C>T	ENSP00000457384.1:n.84-3C>T
ENST00000566347.5:c.354-3C>T	ENSP00000457783.1:n.354-3C>T
ENST00000567060.5:c.298-42C>T	ENSP00000454818.1:n.298-42C>T
NM_017882.2:c.543-3C>T	NP_060352.1:n.543-3C>T
XR_931861.1:n.765-3C>T
NM_017882.3:c.543-3C>T MANE Select	NP_060352.1:n.543-3C>T