Canonical Allele Identifier: CA392973630

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504165T>G (hg19) ; chr15:g.68211827T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211827T>G , CM000677.2:g.68211827T>G	GRCh38
NC_000015.9:g.68504165T>G , CM000677.1:g.68504165T>G	GRCh37
NC_000015.8:g.66291219T>G	NCBI36
NG_008764.2:g.50385A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.334A>C MANE Select	ENSP00000249806.5:p.Ile112Leu
ENST00000562767.2:c.84-14199A>C	ENSP00000456336.1:n.84-14199A>C
ENST00000563917.2:n.176A>C
ENST00000565471.6:c.84-2068A>C	ENSP00000457384.1:n.84-2068A>C
ENST00000635747.1:c.*237A>C	ENSP00000490627.1:n.*237A>C
ENST00000636212.1:c.298-86A>C	ENSP00000489851.1:n.298-86A>C
ENST00000636314.1:c.183-509A>C	ENSP00000490295.1:n.183-509A>C
ENST00000636674.1:n.1317A>C
ENST00000636964.1:n.1506A>C
ENST00000637054.1:c.198+6709A>C	ENSP00000490807.1:n.198+6709A>C
ENST00000637223.1:c.*201-509A>C	ENSP00000490010.1:n.*201-509A>C
ENST00000637329.1:c.303A>C
ENST00000637450.1:c.219A>C	ENSP00000490204.1:p.Pro73=
ENST00000637494.1:c.199-509A>C	ENSP00000490057.1:n.199-509A>C
ENST00000637667.1:c.235A>C	ENSP00000489843.1:p.Ile79Leu
ENST00000637823.1:c.224-184A>C
ENST00000637888.1:c.198+6709A>C	ENSP00000490546.1:n.198+6709A>C
ENST00000638076.1:c.334A>C	ENSP00000490373.1:p.Ile112Leu
ENST00000638144.1:n.130-509A>C
ENST00000646164.1:c.38+6709A>C
ENST00000249806.9:c.334A>C	ENSP00000249806.5:p.Ile112Leu
ENST00000538696.5:c.430A>C	ENSP00000445770.1:p.Ile144Leu
ENST00000562767.1:c.84-14199A>C	ENSP00000456336.1:n.84-14199A>C
ENST00000563917.1:n.115A>C
ENST00000564752.1:c.334A>C	ENSP00000457822.1:p.Ile112Leu
ENST00000565471.5:c.84-2068A>C	ENSP00000457384.1:n.84-2068A>C
ENST00000566347.5:c.298-509A>C	ENSP00000457783.1:n.298-509A>C
ENST00000567060.5:c.298-2107A>C	ENSP00000454818.1:n.298-2107A>C
NM_017882.2:c.334A>C	NP_060352.1:p.Ile112Leu
XR_931861.1:n.437A>C
NM_017882.3:c.334A>C MANE Select	NP_060352.1:p.Ile112Leu