Canonical Allele Identifier: CA392973610

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504156C>G (hg19) ; chr15:g.68211818C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211818C>G , CM000677.2:g.68211818C>G	GRCh38
NC_000015.9:g.68504156C>G , CM000677.1:g.68504156C>G	GRCh37
NC_000015.8:g.66291210C>G	NCBI36
NG_008764.2:g.50394G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.343G>C MANE Select	ENSP00000249806.5:p.Val115Leu
ENST00000562767.2:c.84-14190G>C	ENSP00000456336.1:n.84-14190G>C
ENST00000563917.2:n.185G>C
ENST00000565471.6:c.84-2059G>C	ENSP00000457384.1:n.84-2059G>C
ENST00000635747.1:c.*246G>C	ENSP00000490627.1:n.*246G>C
ENST00000636212.1:c.298-77G>C	ENSP00000489851.1:n.298-77G>C
ENST00000636314.1:c.183-500G>C	ENSP00000490295.1:n.183-500G>C
ENST00000636674.1:n.1326G>C
ENST00000636964.1:n.1515G>C
ENST00000637054.1:c.198+6718G>C	ENSP00000490807.1:n.198+6718G>C
ENST00000637223.1:c.*201-500G>C	ENSP00000490010.1:n.*201-500G>C
ENST00000637329.1:c.312G>C
ENST00000637450.1:c.228G>C	ENSP00000490204.1:p.Thr76=
ENST00000637494.1:c.199-500G>C	ENSP00000490057.1:n.199-500G>C
ENST00000637667.1:c.244G>C	ENSP00000489843.1:p.Val82Leu
ENST00000637823.1:c.224-175G>C
ENST00000637888.1:c.198+6718G>C	ENSP00000490546.1:n.198+6718G>C
ENST00000638076.1:c.343G>C	ENSP00000490373.1:p.Val115Leu
ENST00000638144.1:n.130-500G>C
ENST00000646164.1:c.38+6718G>C
ENST00000249806.9:c.343G>C	ENSP00000249806.5:p.Val115Leu
ENST00000538696.5:c.439G>C	ENSP00000445770.1:p.Val147Leu
ENST00000562767.1:c.84-14190G>C	ENSP00000456336.1:n.84-14190G>C
ENST00000563917.1:n.124G>C
ENST00000564752.1:c.343G>C	ENSP00000457822.1:p.Val115Leu
ENST00000565471.5:c.84-2059G>C	ENSP00000457384.1:n.84-2059G>C
ENST00000566347.5:c.298-500G>C	ENSP00000457783.1:n.298-500G>C
ENST00000567060.5:c.298-2098G>C	ENSP00000454818.1:n.298-2098G>C
NM_017882.2:c.343G>C	NP_060352.1:p.Val115Leu
XR_931861.1:n.446G>C
NM_017882.3:c.343G>C MANE Select	NP_060352.1:p.Val115Leu