Canonical Allele Identifier: CA392971932

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68500620G>T (hg19) ; chr15:g.68208282G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68208282G>T , CM000677.2:g.68208282G>T	GRCh38
NC_000015.9:g.68500620G>T , CM000677.1:g.68500620G>T	GRCh37
NC_000015.8:g.66287674G>T	NCBI36
NG_008764.2:g.53930C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.794C>A MANE Select	ENSP00000249806.5:p.Ser265Tyr
ENST00000562767.2:c.84-10654C>A	ENSP00000456336.1:n.84-10654C>A
ENST00000565471.6:c.335C>A	ENSP00000457384.1:p.Ser112Tyr
ENST00000635747.1:c.*697C>A	ENSP00000490627.1:n.*697C>A
ENST00000636212.1:c.*464C>A	ENSP00000489851.1:n.*464C>A
ENST00000636674.1:n.1896C>A
ENST00000636964.1:n.2322C>A
ENST00000637054.1:c.198+10254C>A	ENSP00000490807.1:n.198+10254C>A
ENST00000637329.1:c.763C>A
ENST00000637450.1:c.*448C>A	ENSP00000490204.1:n.*448C>A
ENST00000637494.1:c.506C>A	ENSP00000490057.1:p.Ser169Tyr
ENST00000637667.1:c.695C>A	ENSP00000489843.1:p.Ser232Tyr
ENST00000637823.1:c.619C>A
ENST00000637888.1:c.198+10254C>A	ENSP00000490546.1:n.198+10254C>A
ENST00000638076.1:c.*397C>A	ENSP00000490373.1:n.*397C>A
ENST00000638144.1:n.437C>A
ENST00000646164.1:c.39-8601C>A
ENST00000249806.9:c.794C>A	ENSP00000249806.5:p.Ser265Tyr
ENST00000538696.5:c.890C>A	ENSP00000445770.1:p.Ser297Tyr
ENST00000562767.1:c.84-10654C>A	ENSP00000456336.1:n.84-10654C>A
ENST00000565471.5:c.335C>A	ENSP00000457384.1:p.Ser112Tyr
ENST00000566347.5:c.605C>A	ENSP00000457783.1:p.Ser202Tyr
ENST00000567060.5:c.*192C>A	ENSP00000454818.1:n.*192C>A
NM_017882.2:c.794C>A	NP_060352.1:p.Ser265Tyr
NM_017882.3:c.794C>A MANE Select	NP_060352.1:p.Ser265Tyr