Canonical Allele Identifier: CA490912684

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504052A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211714A>T , CM000677.2:g.68211714A>T	GRCh38
NC_000015.9:g.68504052A>T , CM000677.1:g.68504052A>T	GRCh37
NC_000015.8:g.66291106A>T	NCBI36
NG_008764.2:g.50498T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.447T>A MANE Select	ENSP00000249806.5:p.Arg149=
ENST00000562767.2:c.84-14086T>A	ENSP00000456336.1:n.84-14086T>A
ENST00000563917.2:n.289T>A
ENST00000565471.6:c.84-1955T>A	ENSP00000457384.1:n.84-1955T>A
ENST00000635747.1:c.*350T>A	ENSP00000490627.1:n.*350T>A
ENST00000636212.1:c.325T>A	ENSP00000489851.1:p.Ter109Arg
ENST00000636314.1:c.183-396T>A	ENSP00000490295.1:n.183-396T>A
ENST00000636674.1:n.1430T>A
ENST00000636964.1:n.1619T>A
ENST00000637054.1:c.198+6822T>A	ENSP00000490807.1:n.198+6822T>A
ENST00000637223.1:c.*201-396T>A	ENSP00000490010.1:n.*201-396T>A
ENST00000637329.1:c.416T>A
ENST00000637450.1:c.*101T>A	ENSP00000490204.1:n.*101T>A
ENST00000637494.1:c.199-396T>A	ENSP00000490057.1:n.199-396T>A
ENST00000637667.1:c.348T>A	ENSP00000489843.1:p.Arg116=
ENST00000637823.1:c.224-71T>A
ENST00000637888.1:c.198+6822T>A	ENSP00000490546.1:n.198+6822T>A
ENST00000638076.1:c.447T>A	ENSP00000490373.1:p.Arg149=
ENST00000638144.1:n.130-396T>A
ENST00000646164.1:c.38+6822T>A
ENST00000249806.9:c.447T>A	ENSP00000249806.5:p.Arg149=
ENST00000538696.5:c.543T>A	ENSP00000445770.1:p.Arg181=
ENST00000562767.1:c.84-14086T>A	ENSP00000456336.1:n.84-14086T>A
ENST00000563917.1:n.228T>A
ENST00000564752.1:c.447T>A	ENSP00000457822.1:p.Arg149=
ENST00000565471.5:c.84-1955T>A	ENSP00000457384.1:n.84-1955T>A
ENST00000566347.5:c.298-396T>A	ENSP00000457783.1:n.298-396T>A
ENST00000567060.5:c.298-1994T>A	ENSP00000454818.1:n.298-1994T>A
NM_017882.2:c.447T>A	NP_060352.1:p.Arg149=
XR_931861.1:n.550T>A
NM_017882.3:c.447T>A MANE Select	NP_060352.1:p.Arg149=