Canonical Allele Identifier: CA392973053

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68502091G>C (hg19) ; chr15:g.68209753G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209753G>C , CM000677.2:g.68209753G>C	GRCh38
NC_000015.9:g.68502091G>C , CM000677.1:g.68502091G>C	GRCh37
NC_000015.8:g.66289145G>C	NCBI36
NG_008764.2:g.52459C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.549C>G MANE Select	ENSP00000249806.5:p.Ile183Met
ENST00000562767.2:c.84-12125C>G	ENSP00000456336.1:n.84-12125C>G
ENST00000563917.2:n.391C>G
ENST00000565471.6:c.90C>G	ENSP00000457384.1:p.Ile30Met
ENST00000635747.1:c.*452C>G	ENSP00000490627.1:n.*452C>G
ENST00000636212.1:c.*219C>G	ENSP00000489851.1:n.*219C>G
ENST00000636314.1:c.245C>G	ENSP00000490295.1:p.Ser82Cys
ENST00000636674.1:n.1651C>G
ENST00000636964.1:n.2077C>G
ENST00000637054.1:c.198+8783C>G	ENSP00000490807.1:n.198+8783C>G
ENST00000637223.1:c.*263C>G	ENSP00000490010.1:n.*263C>G
ENST00000637329.1:c.518C>G
ENST00000637450.1:c.*203C>G	ENSP00000490204.1:n.*203C>G
ENST00000637494.1:c.261C>G	ENSP00000490057.1:p.Ile87Met
ENST00000637667.1:c.450C>G	ENSP00000489843.1:p.Ile150Met
ENST00000637823.1:c.374C>G
ENST00000637888.1:c.198+8783C>G	ENSP00000490546.1:n.198+8783C>G
ENST00000638076.1:c.*152C>G	ENSP00000490373.1:n.*152C>G
ENST00000638144.1:n.192C>G
ENST00000646164.1:c.38+8783C>G
ENST00000249806.9:c.549C>G	ENSP00000249806.5:p.Ile183Met
ENST00000538696.5:c.645C>G	ENSP00000445770.1:p.Ile215Met
ENST00000562767.1:c.84-12125C>G	ENSP00000456336.1:n.84-12125C>G
ENST00000563917.1:n.449C>G
ENST00000564752.1:c.575C>G	ENSP00000457822.1:p.Ser192Cys
ENST00000565471.5:c.90C>G	ENSP00000457384.1:p.Ile30Met
ENST00000566347.5:c.360C>G	ENSP00000457783.1:p.Ile120Met
ENST00000567060.5:c.298-33C>G	ENSP00000454818.1:n.298-33C>G
NM_017882.2:c.549C>G	NP_060352.1:p.Ile183Met
XR_931861.1:n.771C>G
NM_017882.3:c.549C>G MANE Select	NP_060352.1:p.Ile183Met