Canonical Allele Identifier: CA392972922

Gene: CLN6

Linked Data

• MyVariant Identifiers: chr15:g.68502043G>A (hg19) ; chr15:g.68209705G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209705G>A , CM000677.2:g.68209705G>A	GRCh38
NC_000015.9:g.68502043G>A , CM000677.1:g.68502043G>A	GRCh37
NC_000015.8:g.66289097G>A	NCBI36
NG_008764.2:g.52507C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.597C>T MANE Select	ENSP00000249806.5:p.Ala199=
ENST00000562767.2:c.84-12077C>T	ENSP00000456336.1:n.84-12077C>T
ENST00000563917.2:n.439C>T
ENST00000565471.6:c.138C>T	ENSP00000457384.1:p.Ala46=
ENST00000635747.1:c.*500C>T	ENSP00000490627.1:n.*500C>T
ENST00000636212.1:c.*267C>T	ENSP00000489851.1:n.*267C>T
ENST00000636314.1:c.293C>T	ENSP00000490295.1:p.Pro98Leu
ENST00000636674.1:n.1699C>T
ENST00000636964.1:n.2125C>T
ENST00000637054.1:c.198+8831C>T	ENSP00000490807.1:n.198+8831C>T
ENST00000637223.1:c.*311C>T	ENSP00000490010.1:n.*311C>T
ENST00000637329.1:c.566C>T
ENST00000637450.1:c.*251C>T	ENSP00000490204.1:n.*251C>T
ENST00000637494.1:c.309C>T	ENSP00000490057.1:p.Ala103=
ENST00000637667.1:c.498C>T	ENSP00000489843.1:p.Ala166=
ENST00000637823.1:c.422C>T
ENST00000637888.1:c.198+8831C>T	ENSP00000490546.1:n.198+8831C>T
ENST00000638076.1:c.*200C>T	ENSP00000490373.1:n.*200C>T
ENST00000638144.1:n.240C>T
ENST00000646164.1:c.38+8831C>T
ENST00000249806.9:c.597C>T	ENSP00000249806.5:p.Ala199=
ENST00000538696.5:c.693C>T	ENSP00000445770.1:p.Ala231=
ENST00000562767.1:c.84-12077C>T	ENSP00000456336.1:n.84-12077C>T
ENST00000563917.1:n.497C>T
ENST00000564752.1:c.623C>T	ENSP00000457822.1:p.Pro208Leu
ENST00000565471.5:c.138C>T	ENSP00000457384.1:p.Ala46=
ENST00000566347.5:c.408C>T	ENSP00000457783.1:p.Ala136=
ENST00000567060.5:c.313C>T	ENSP00000454818.1:p.Leu105Phe
NM_017882.2:c.597C>T	NP_060352.1:p.Ala199=
XR_931861.1:n.819C>T
NM_017882.3:c.597C>T MANE Select	NP_060352.1:p.Ala199=