Canonical Allele Identifier: CA392973554

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504131C>G (hg19) ; chr15:g.68211793C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211793C>G , CM000677.2:g.68211793C>G	GRCh38
NC_000015.9:g.68504131C>G , CM000677.1:g.68504131C>G	GRCh37
NC_000015.8:g.66291185C>G	NCBI36
NG_008764.2:g.50419G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.368G>C MANE Select	ENSP00000249806.5:p.Gly123Ala
ENST00000562767.2:c.84-14165G>C	ENSP00000456336.1:n.84-14165G>C
ENST00000563917.2:n.210G>C
ENST00000565471.6:c.84-2034G>C	ENSP00000457384.1:n.84-2034G>C
ENST00000635747.1:c.*271G>C	ENSP00000490627.1:n.*271G>C
ENST00000636212.1:c.298-52G>C	ENSP00000489851.1:n.298-52G>C
ENST00000636314.1:c.183-475G>C	ENSP00000490295.1:n.183-475G>C
ENST00000636674.1:n.1351G>C
ENST00000636964.1:n.1540G>C
ENST00000637054.1:c.198+6743G>C	ENSP00000490807.1:n.198+6743G>C
ENST00000637223.1:c.*201-475G>C	ENSP00000490010.1:n.*201-475G>C
ENST00000637329.1:c.337G>C
ENST00000637450.1:c.*22G>C	ENSP00000490204.1:n.*22G>C
ENST00000637494.1:c.199-475G>C	ENSP00000490057.1:n.199-475G>C
ENST00000637667.1:c.269G>C	ENSP00000489843.1:p.Gly90Ala
ENST00000637823.1:c.224-150G>C
ENST00000637888.1:c.198+6743G>C	ENSP00000490546.1:n.198+6743G>C
ENST00000638076.1:c.368G>C	ENSP00000490373.1:p.Gly123Ala
ENST00000638144.1:n.130-475G>C
ENST00000646164.1:c.38+6743G>C
ENST00000249806.9:c.368G>C	ENSP00000249806.5:p.Gly123Ala
ENST00000538696.5:c.464G>C	ENSP00000445770.1:p.Gly155Ala
ENST00000562767.1:c.84-14165G>C	ENSP00000456336.1:n.84-14165G>C
ENST00000563917.1:n.149G>C
ENST00000564752.1:c.368G>C	ENSP00000457822.1:p.Gly123Ala
ENST00000565471.5:c.84-2034G>C	ENSP00000457384.1:n.84-2034G>C
ENST00000566347.5:c.298-475G>C	ENSP00000457783.1:n.298-475G>C
ENST00000567060.5:c.298-2073G>C	ENSP00000454818.1:n.298-2073G>C
NM_017882.2:c.368G>C	NP_060352.1:p.Gly123Ala
XR_931861.1:n.471G>C
NM_017882.3:c.368G>C MANE Select	NP_060352.1:p.Gly123Ala