Canonical Allele Identifier: CA392973369

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68504045G>C (hg19) ; chr15:g.68211707G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211707G>C , CM000677.2:g.68211707G>C	GRCh38
NC_000015.9:g.68504045G>C , CM000677.1:g.68504045G>C	GRCh37
NC_000015.8:g.66291099G>C	NCBI36
NG_008764.2:g.50505C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.454C>G MANE Select	ENSP00000249806.5:p.Pro152Ala
ENST00000562767.2:c.84-14079C>G	ENSP00000456336.1:n.84-14079C>G
ENST00000563917.2:n.296C>G
ENST00000565471.6:c.84-1948C>G	ENSP00000457384.1:n.84-1948C>G
ENST00000635747.1:c.*357C>G	ENSP00000490627.1:n.*357C>G
ENST00000636212.1:c.*5C>G	ENSP00000489851.1:n.*5C>G
ENST00000636314.1:c.183-389C>G	ENSP00000490295.1:n.183-389C>G
ENST00000636674.1:n.1437C>G
ENST00000636964.1:n.1626C>G
ENST00000637054.1:c.198+6829C>G	ENSP00000490807.1:n.198+6829C>G
ENST00000637223.1:c.*201-389C>G	ENSP00000490010.1:n.*201-389C>G
ENST00000637329.1:c.423C>G
ENST00000637450.1:c.*108C>G	ENSP00000490204.1:n.*108C>G
ENST00000637494.1:c.199-389C>G	ENSP00000490057.1:n.199-389C>G
ENST00000637667.1:c.355C>G	ENSP00000489843.1:p.Pro119Ala
ENST00000637823.1:c.224-64C>G
ENST00000637888.1:c.198+6829C>G	ENSP00000490546.1:n.198+6829C>G
ENST00000638076.1:c.454C>G	ENSP00000490373.1:p.Pro152Ala
ENST00000638144.1:n.130-389C>G
ENST00000646164.1:c.38+6829C>G
ENST00000249806.9:c.454C>G	ENSP00000249806.5:p.Pro152Ala
ENST00000538696.5:c.550C>G	ENSP00000445770.1:p.Pro184Ala
ENST00000562767.1:c.84-14079C>G	ENSP00000456336.1:n.84-14079C>G
ENST00000563917.1:n.235C>G
ENST00000564752.1:c.454C>G	ENSP00000457822.1:p.Pro152Ala
ENST00000565471.5:c.84-1948C>G	ENSP00000457384.1:n.84-1948C>G
ENST00000566347.5:c.298-389C>G	ENSP00000457783.1:n.298-389C>G
ENST00000567060.5:c.298-1987C>G	ENSP00000454818.1:n.298-1987C>G
NM_017882.2:c.454C>G	NP_060352.1:p.Pro152Ala
XR_931861.1:n.557C>G
NM_017882.3:c.454C>G MANE Select	NP_060352.1:p.Pro152Ala