Canonical Allele Identifier: CA392973636

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504170C>G (hg19) ; chr15:g.68211832C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211832C>G , CM000677.2:g.68211832C>G	GRCh38
NC_000015.9:g.68504170C>G , CM000677.1:g.68504170C>G	GRCh37
NC_000015.8:g.66291224C>G	NCBI36
NG_008764.2:g.50380G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.329G>C MANE Select	ENSP00000249806.5:p.Arg110Pro
ENST00000562767.2:c.84-14204G>C	ENSP00000456336.1:n.84-14204G>C
ENST00000563917.2:n.171G>C
ENST00000565471.6:c.84-2073G>C	ENSP00000457384.1:n.84-2073G>C
ENST00000635747.1:c.*232G>C	ENSP00000490627.1:n.*232G>C
ENST00000636212.1:c.298-91G>C	ENSP00000489851.1:n.298-91G>C
ENST00000636314.1:c.183-514G>C	ENSP00000490295.1:n.183-514G>C
ENST00000636674.1:n.1312G>C
ENST00000636964.1:n.1501G>C
ENST00000637054.1:c.198+6704G>C	ENSP00000490807.1:n.198+6704G>C
ENST00000637223.1:c.*201-514G>C	ENSP00000490010.1:n.*201-514G>C
ENST00000637329.1:c.298G>C
ENST00000637450.1:c.214G>C	ENSP00000490204.1:p.Ala72Pro
ENST00000637494.1:c.199-514G>C	ENSP00000490057.1:n.199-514G>C
ENST00000637667.1:c.230G>C	ENSP00000489843.1:p.Arg77Pro
ENST00000637823.1:c.224-189G>C
ENST00000637888.1:c.198+6704G>C	ENSP00000490546.1:n.198+6704G>C
ENST00000638076.1:c.329G>C	ENSP00000490373.1:p.Arg110Pro
ENST00000638144.1:n.130-514G>C
ENST00000646164.1:c.38+6704G>C
ENST00000249806.9:c.329G>C	ENSP00000249806.5:p.Arg110Pro
ENST00000538696.5:c.425G>C	ENSP00000445770.1:p.Arg142Pro
ENST00000562767.1:c.84-14204G>C	ENSP00000456336.1:n.84-14204G>C
ENST00000563917.1:n.110G>C
ENST00000564752.1:c.329G>C	ENSP00000457822.1:p.Arg110Pro
ENST00000565471.5:c.84-2073G>C	ENSP00000457384.1:n.84-2073G>C
ENST00000566347.5:c.298-514G>C	ENSP00000457783.1:n.298-514G>C
ENST00000567060.5:c.298-2112G>C	ENSP00000454818.1:n.298-2112G>C
NM_017882.2:c.329G>C	NP_060352.1:p.Arg110Pro
XR_931861.1:n.432G>C
NM_017882.3:c.329G>C MANE Select	NP_060352.1:p.Arg110Pro