Canonical Allele Identifier: CA392974362

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68506654C>A (hg19) ; chr15:g.68214316C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68214316C>A , CM000677.2:g.68214316C>A	GRCh38
NC_000015.9:g.68506654C>A , CM000677.1:g.68506654C>A	GRCh37
NC_000015.8:g.66293708C>A	NCBI36
NG_008764.2:g.47896G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.271G>T MANE Select	ENSP00000249806.5:p.Val91Phe
ENST00000562767.2:c.83+15186G>T	ENSP00000456336.1:n.83+15186G>T
ENST00000563917.2:n.113G>T
ENST00000565471.6:c.84-4557G>T	ENSP00000457384.1:n.84-4557G>T
ENST00000635747.1:c.*174G>T	ENSP00000490627.1:n.*174G>T
ENST00000635754.1:n.1293G>T
ENST00000636020.1:n.403G>T
ENST00000636212.1:c.271G>T	ENSP00000489851.1:p.Val91Phe
ENST00000636314.1:c.156G>T	ENSP00000490295.1:p.Thr52=
ENST00000637054.1:c.198+4220G>T	ENSP00000490807.1:n.198+4220G>T
ENST00000637223.1:c.*174G>T	ENSP00000490010.1:n.*174G>T
ENST00000637329.1:c.182G>T
ENST00000637450.1:c.156G>T	ENSP00000490204.1:p.Thr52=
ENST00000637494.1:c.199-2998G>T	ENSP00000490057.1:n.199-2998G>T
ENST00000637667.1:c.199-2453G>T	ENSP00000489843.1:n.199-2453G>T
ENST00000637823.1:c.197G>T
ENST00000637888.1:c.198+4220G>T	ENSP00000490546.1:n.198+4220G>T
ENST00000638076.1:c.271G>T	ENSP00000490373.1:p.Val91Phe
ENST00000638144.1:n.103G>T
ENST00000646164.1:c.38+4220G>T
ENST00000249806.9:c.271G>T	ENSP00000249806.5:p.Val91Phe
ENST00000538696.5:c.367G>T	ENSP00000445770.1:p.Val123Phe
ENST00000562767.1:c.83+15186G>T	ENSP00000456336.1:n.83+15186G>T
ENST00000563917.1:n.52G>T
ENST00000564752.1:c.271G>T	ENSP00000457822.1:p.Val91Phe
ENST00000564846.1:n.703G>T
ENST00000565471.5:c.84-4557G>T	ENSP00000457384.1:n.84-4557G>T
ENST00000566347.5:c.271G>T	ENSP00000457783.1:p.Val91Phe
ENST00000567060.5:c.271G>T	ENSP00000454818.1:p.Val91Phe
NM_017882.2:c.271G>T	NP_060352.1:p.Val91Phe
XR_931861.1:n.374G>T
NM_017882.3:c.271G>T MANE Select	NP_060352.1:p.Val91Phe