Canonical Allele Identifier: CA272387549

Gene: CLN6

Linked Data

• dbSNP Id: rs553192210
• gnomAD v3: 15-68214177-C-A
• gnomAD v4: 15-68214177-C-A
• MyVariant Identifiers: chr15:g.68506515C>A (hg19) ; chr15:g.68214177C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68214177C>A , CM000677.2:g.68214177C>A	GRCh38
NC_000015.9:g.68506515C>A , CM000677.1:g.68506515C>A	GRCh37
NC_000015.8:g.66293569C>A	NCBI36
NG_008764.2:g.48035G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.297+113G>T MANE Select	ENSP00000249806.5:n.297+113G>T
ENST00000562767.2:c.83+15325G>T	ENSP00000456336.1:n.83+15325G>T
ENST00000563917.2:n.139+113G>T
ENST00000565471.6:c.84-4418G>T	ENSP00000457384.1:n.84-4418G>T
ENST00000635747.1:c.*200+113G>T	ENSP00000490627.1:n.*200+113G>T
ENST00000635754.1:n.1432G>T
ENST00000636020.1:n.542G>T
ENST00000636212.1:c.297+113G>T	ENSP00000489851.1:n.297+113G>T
ENST00000636314.1:c.182+113G>T	ENSP00000490295.1:n.182+113G>T
ENST00000637054.1:c.198+4359G>T	ENSP00000490807.1:n.198+4359G>T
ENST00000637223.1:c.*200+113G>T	ENSP00000490010.1:n.*200+113G>T
ENST00000637329.1:c.208+113G>T
ENST00000637450.1:c.182+113G>T	ENSP00000490204.1:n.182+113G>T
ENST00000637494.1:c.199-2859G>T	ENSP00000490057.1:n.199-2859G>T
ENST00000637667.1:c.199-2314G>T	ENSP00000489843.1:n.199-2314G>T
ENST00000637823.1:c.223+113G>T
ENST00000637888.1:c.198+4359G>T	ENSP00000490546.1:n.198+4359G>T
ENST00000638076.1:c.297+113G>T	ENSP00000490373.1:n.297+113G>T
ENST00000638144.1:n.129+113G>T
ENST00000646164.1:c.38+4359G>T
ENST00000249806.9:c.297+113G>T	ENSP00000249806.5:n.297+113G>T
ENST00000538696.5:c.393+113G>T	ENSP00000445770.1:n.393+113G>T
ENST00000562767.1:c.83+15325G>T	ENSP00000456336.1:n.83+15325G>T
ENST00000563917.1:n.78+113G>T
ENST00000564752.1:c.297+113G>T	ENSP00000457822.1:n.297+113G>T
ENST00000564846.1:n.842G>T
ENST00000565471.5:c.84-4418G>T	ENSP00000457384.1:n.84-4418G>T
ENST00000566347.5:c.297+113G>T	ENSP00000457783.1:n.297+113G>T
ENST00000567060.5:c.297+113G>T	ENSP00000454818.1:n.297+113G>T
NM_017882.2:c.297+113G>T	NP_060352.1:n.297+113G>T
XR_931861.1:n.400+113G>T
NM_017882.3:c.297+113G>T MANE Select	NP_060352.1:n.297+113G>T