Canonical Allele Identifier: CA2184879510
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68209660C= , CM000677.2:g.68209660C= GRCh38
NC_000015.9:g.68501998C= , CM000677.1:g.68501998C= GRCh37
NC_000015.8:g.66289052C= NCBI36
NG_008764.2:g.52552G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.642G= MANE Select ENSP00000249806.5:p.Val214=
ENST00000562767.2:c.84-12032G= ENSP00000456336.1:n.84-12032G=
ENST00000563917.2:n.484G=
ENST00000565471.6:c.183G= ENSP00000457384.1:p.Val61=
ENST00000635747.1:c.*545G= ENSP00000490627.1:n.*545G=
ENST00000636212.1:c.*312G= ENSP00000489851.1:n.*312G=
ENST00000636674.1:n.1744G=
ENST00000636964.1:n.2170G=
ENST00000637054.1:c.198+8876G= ENSP00000490807.1:n.198+8876G=
ENST00000637329.1:c.611G=
ENST00000637450.1:c.*296G= ENSP00000490204.1:n.*296G=
ENST00000637494.1:c.354G= ENSP00000490057.1:p.Val118=
ENST00000637667.1:c.543G= ENSP00000489843.1:p.Val181=
ENST00000637823.1:c.467G=
ENST00000637888.1:c.198+8876G= ENSP00000490546.1:n.198+8876G=
ENST00000638076.1:c.*245G= ENSP00000490373.1:n.*245G=
ENST00000638144.1:n.285G=
ENST00000646164.1:c.38+8876G=
ENST00000249806.9:c.642G= ENSP00000249806.5:p.Val214=
ENST00000538696.5:c.738G= ENSP00000445770.1:p.Val246=
ENST00000562767.1:c.84-12032G= ENSP00000456336.1:n.84-12032G=
ENST00000563917.1:n.542G=
ENST00000564752.1:c.*26G= ENSP00000457822.1:n.*26G=
ENST00000565471.5:c.183G= ENSP00000457384.1:p.Val61=
ENST00000566347.5:c.453G= ENSP00000457783.1:p.Val151=
ENST00000567060.5:c.*40G= ENSP00000454818.1:n.*40G=
NM_017882.2:c.642G= NP_060352.1:p.Val214=
XR_931861.1:n.864G=
NM_017882.3:c.642G= MANE Select NP_060352.1:p.Val214=