Canonical Allele Identifier: CA392971992

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68500648C>A (hg19) ; chr15:g.68208310C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68208310C>A , CM000677.2:g.68208310C>A	GRCh38
NC_000015.9:g.68500648C>A , CM000677.1:g.68500648C>A	GRCh37
NC_000015.8:g.66287702C>A	NCBI36
NG_008764.2:g.53902G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.766G>T MANE Select	ENSP00000249806.5:p.Asp256Tyr
ENST00000562767.2:c.84-10682G>T	ENSP00000456336.1:n.84-10682G>T
ENST00000565471.6:c.307G>T	ENSP00000457384.1:p.Asp103Tyr
ENST00000635747.1:c.*669G>T	ENSP00000490627.1:n.*669G>T
ENST00000636212.1:c.*436G>T	ENSP00000489851.1:n.*436G>T
ENST00000636674.1:n.1868G>T
ENST00000636964.1:n.2294G>T
ENST00000637054.1:c.198+10226G>T	ENSP00000490807.1:n.198+10226G>T
ENST00000637329.1:c.735G>T
ENST00000637450.1:c.*420G>T	ENSP00000490204.1:n.*420G>T
ENST00000637494.1:c.478G>T	ENSP00000490057.1:p.Asp160Tyr
ENST00000637667.1:c.667G>T	ENSP00000489843.1:p.Asp223Tyr
ENST00000637823.1:c.591G>T
ENST00000637888.1:c.198+10226G>T	ENSP00000490546.1:n.198+10226G>T
ENST00000638076.1:c.*369G>T	ENSP00000490373.1:n.*369G>T
ENST00000638144.1:n.409G>T
ENST00000646164.1:c.39-8629G>T
ENST00000249806.9:c.766G>T	ENSP00000249806.5:p.Asp256Tyr
ENST00000538696.5:c.862G>T	ENSP00000445770.1:p.Asp288Tyr
ENST00000562767.1:c.84-10682G>T	ENSP00000456336.1:n.84-10682G>T
ENST00000565471.5:c.307G>T	ENSP00000457384.1:p.Asp103Tyr
ENST00000566347.5:c.577G>T	ENSP00000457783.1:p.Asp193Tyr
ENST00000567060.5:c.*164G>T	ENSP00000454818.1:n.*164G>T
NM_017882.2:c.766G>T	NP_060352.1:p.Asp256Tyr
NM_017882.3:c.766G>T MANE Select	NP_060352.1:p.Asp256Tyr