Canonical Allele Identifier: CA715171537

Gene: CLN6

Linked Data

• dbSNP Id: rs1201875953
• gnomAD v3: 15-68211943-T-G
• gnomAD v4: 15-68211943-T-G
• MyVariant Identifiers: chr15:g.68504281T>G (hg19) ; chr15:g.68211943T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211943T>G , CM000677.2:g.68211943T>G	GRCh38
NC_000015.9:g.68504281T>G , CM000677.1:g.68504281T>G	GRCh37
NC_000015.8:g.66291335T>G	NCBI36
NG_008764.2:g.50269A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.298-80A>C MANE Select	ENSP00000249806.5:n.298-80A>C
ENST00000562767.2:c.84-14315A>C	ENSP00000456336.1:n.84-14315A>C
ENST00000563917.2:n.140-80A>C
ENST00000565471.6:c.84-2184A>C	ENSP00000457384.1:n.84-2184A>C
ENST00000635747.1:c.*201-80A>C	ENSP00000490627.1:n.*201-80A>C
ENST00000636212.1:c.298-202A>C	ENSP00000489851.1:n.298-202A>C
ENST00000636314.1:c.183-625A>C	ENSP00000490295.1:n.183-625A>C
ENST00000636674.1:n.1201A>C
ENST00000636964.1:n.1390A>C
ENST00000637054.1:c.198+6593A>C	ENSP00000490807.1:n.198+6593A>C
ENST00000637223.1:c.*201-625A>C	ENSP00000490010.1:n.*201-625A>C
ENST00000637329.1:c.209-22A>C
ENST00000637450.1:c.183-80A>C	ENSP00000490204.1:n.183-80A>C
ENST00000637494.1:c.199-625A>C	ENSP00000490057.1:n.199-625A>C
ENST00000637667.1:c.199-80A>C	ENSP00000489843.1:n.199-80A>C
ENST00000637823.1:c.224-300A>C
ENST00000637888.1:c.198+6593A>C	ENSP00000490546.1:n.198+6593A>C
ENST00000638076.1:c.298-80A>C	ENSP00000490373.1:n.298-80A>C
ENST00000638144.1:n.130-625A>C
ENST00000646164.1:c.38+6593A>C
ENST00000249806.9:c.298-80A>C	ENSP00000249806.5:n.298-80A>C
ENST00000538696.5:c.394-80A>C	ENSP00000445770.1:n.394-80A>C
ENST00000562767.1:c.84-14315A>C	ENSP00000456336.1:n.84-14315A>C
ENST00000563917.1:n.79-80A>C
ENST00000564752.1:c.298-80A>C	ENSP00000457822.1:n.298-80A>C
ENST00000565471.5:c.84-2184A>C	ENSP00000457384.1:n.84-2184A>C
ENST00000566347.5:c.298-625A>C	ENSP00000457783.1:n.298-625A>C
ENST00000567060.5:c.298-2223A>C	ENSP00000454818.1:n.298-2223A>C
NM_017882.2:c.298-80A>C	NP_060352.1:n.298-80A>C
XR_931861.1:n.401-80A>C
NM_017882.3:c.298-80A>C MANE Select	NP_060352.1:n.298-80A>C