Canonical Allele Identifier: CA392973304

Gene: CLN6

Linked Data

• gnomAD v4: 15-68211677-G-T
• MyVariant Identifiers: chr15:g.68504015G>T (hg19) ; chr15:g.68211677G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211677G>T , CM000677.2:g.68211677G>T	GRCh38
NC_000015.9:g.68504015G>T , CM000677.1:g.68504015G>T	GRCh37
NC_000015.8:g.66291069G>T	NCBI36
NG_008764.2:g.50535C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.484C>A MANE Select	ENSP00000249806.5:p.Leu162Met
ENST00000562767.2:c.84-14049C>A	ENSP00000456336.1:n.84-14049C>A
ENST00000563917.2:n.326C>A
ENST00000565471.6:c.84-1918C>A	ENSP00000457384.1:n.84-1918C>A
ENST00000635747.1:c.*387C>A	ENSP00000490627.1:n.*387C>A
ENST00000636212.1:c.*35C>A	ENSP00000489851.1:n.*35C>A
ENST00000636314.1:c.183-359C>A	ENSP00000490295.1:n.183-359C>A
ENST00000636674.1:n.1467C>A
ENST00000636964.1:n.1656C>A
ENST00000637054.1:c.198+6859C>A	ENSP00000490807.1:n.198+6859C>A
ENST00000637223.1:c.*201-359C>A	ENSP00000490010.1:n.*201-359C>A
ENST00000637329.1:c.453C>A
ENST00000637450.1:c.*138C>A	ENSP00000490204.1:n.*138C>A
ENST00000637494.1:c.199-359C>A	ENSP00000490057.1:n.199-359C>A
ENST00000637667.1:c.385C>A	ENSP00000489843.1:p.Leu129Met
ENST00000637823.1:c.224-34C>A
ENST00000637888.1:c.198+6859C>A	ENSP00000490546.1:n.198+6859C>A
ENST00000638076.1:c.484C>A	ENSP00000490373.1:p.Leu162Met
ENST00000638144.1:n.130-359C>A
ENST00000646164.1:c.38+6859C>A
ENST00000249806.9:c.484C>A	ENSP00000249806.5:p.Leu162Met
ENST00000538696.5:c.580C>A	ENSP00000445770.1:p.Leu194Met
ENST00000562767.1:c.84-14049C>A	ENSP00000456336.1:n.84-14049C>A
ENST00000563917.1:n.265C>A
ENST00000564752.1:c.484C>A	ENSP00000457822.1:p.Leu162Met
ENST00000565471.5:c.84-1918C>A	ENSP00000457384.1:n.84-1918C>A
ENST00000566347.5:c.298-359C>A	ENSP00000457783.1:n.298-359C>A
ENST00000567060.5:c.298-1957C>A	ENSP00000454818.1:n.298-1957C>A
NM_017882.2:c.484C>A	NP_060352.1:p.Leu162Met
XR_931861.1:n.587C>A
NM_017882.3:c.484C>A MANE Select	NP_060352.1:p.Leu162Met