Canonical Allele Identifier: CA7630541
Gene: CLN6 HGNC NCBI

Linked Data

dbSNP Id: rs752617180

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68209779G>A , CM000677.2:g.68209779G>A GRCh38
NC_000015.9:g.68502117G>A , CM000677.1:g.68502117G>A GRCh37
NC_000015.8:g.66289171G>A NCBI36
NG_008764.2:g.52433C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.543-20C>T MANE Select ENSP00000249806.5:n.543-20C>T
ENST00000562767.2:c.84-12151C>T ENSP00000456336.1:n.84-12151C>T
ENST00000563917.2:n.385-20C>T
ENST00000565471.6:c.84-20C>T ENSP00000457384.1:n.84-20C>T
ENST00000635747.1:c.*446-20C>T ENSP00000490627.1:n.*446-20C>T
ENST00000636212.1:c.*213-20C>T ENSP00000489851.1:n.*213-20C>T
ENST00000636314.1:c.239-20C>T ENSP00000490295.1:n.239-20C>T
ENST00000636674.1:n.1645-20C>T
ENST00000636964.1:n.2071-20C>T
ENST00000637054.1:c.198+8757C>T ENSP00000490807.1:n.198+8757C>T
ENST00000637223.1:c.*257-20C>T ENSP00000490010.1:n.*257-20C>T
ENST00000637329.1:c.512-20C>T
ENST00000637450.1:c.*197-20C>T ENSP00000490204.1:n.*197-20C>T
ENST00000637494.1:c.255-20C>T ENSP00000490057.1:n.255-20C>T
ENST00000637667.1:c.444-20C>T ENSP00000489843.1:n.444-20C>T
ENST00000637823.1:c.368-20C>T
ENST00000637888.1:c.198+8757C>T ENSP00000490546.1:n.198+8757C>T
ENST00000638076.1:c.*146-20C>T ENSP00000490373.1:n.*146-20C>T
ENST00000638144.1:n.186-20C>T
ENST00000646164.1:c.38+8757C>T
ENST00000249806.9:c.543-20C>T ENSP00000249806.5:n.543-20C>T
ENST00000538696.5:c.639-20C>T ENSP00000445770.1:n.639-20C>T
ENST00000562767.1:c.84-12151C>T ENSP00000456336.1:n.84-12151C>T
ENST00000563917.1:n.443-20C>T
ENST00000564752.1:c.569-20C>T ENSP00000457822.1:n.569-20C>T
ENST00000565471.5:c.84-20C>T ENSP00000457384.1:n.84-20C>T
ENST00000566347.5:c.354-20C>T ENSP00000457783.1:n.354-20C>T
ENST00000567060.5:c.298-59C>T ENSP00000454818.1:n.298-59C>T
NM_017882.2:c.543-20C>T NP_060352.1:n.543-20C>T
XR_931861.1:n.765-20C>T
NM_017882.3:c.543-20C>T MANE Select NP_060352.1:n.543-20C>T