Canonical Allele Identifier: CA2184879879
Gene: CLN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68209884_68209886delinsTGA , CM000677.2:g.68209884_68209886delinsTGA GRCh38
NC_000015.9:g.68502222_68502224delinsTGA , CM000677.1:g.68502222_68502224delinsTGA GRCh37
NC_000015.8:g.66289276_66289278delinsTGA NCBI36
NG_008764.2:g.52326_52328delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000249806.11:c.543-127_543-125delinsTCA MANE Select ENSP00000249806.5:n.543-127_543-125delinsTCA
ENST00000562767.2:c.84-12258_84-12256delinsTCA ENSP00000456336.1:n.84-12258_84-12256delinsTCA
ENST00000563917.2:n.385-127_385-125delinsTCA
ENST00000565471.6:c.84-127_84-125delinsTCA ENSP00000457384.1:n.84-127_84-125delinsTCA
ENST00000635747.1:c.*446-127_*446-125delinsTCA ENSP00000490627.1:n.*446-127_*446-125delinsTCA
ENST00000636212.1:c.*213-127_*213-125delinsTCA ENSP00000489851.1:n.*213-127_*213-125delinsTCA
ENST00000636314.1:c.239-127_239-125delinsTCA ENSP00000490295.1:n.239-127_239-125delinsTCA
ENST00000636674.1:n.1645-127_1645-125delinsTCA
ENST00000636964.1:n.2071-127_2071-125delinsTCA
ENST00000637054.1:c.198+8650_198+8652delinsTCA ENSP00000490807.1:n.198+8650_198+8652delinsTCA
ENST00000637223.1:c.*257-127_*257-125delinsTCA ENSP00000490010.1:n.*257-127_*257-125delinsTCA
ENST00000637329.1:c.512-127_512-125delinsTCA
ENST00000637450.1:c.*197-127_*197-125delinsTCA ENSP00000490204.1:n.*197-127_*197-125delinsTCA
ENST00000637494.1:c.255-127_255-125delinsTCA ENSP00000490057.1:n.255-127_255-125delinsTCA
ENST00000637667.1:c.444-127_444-125delinsTCA ENSP00000489843.1:n.444-127_444-125delinsTCA
ENST00000637823.1:c.368-127_368-125delinsTCA
ENST00000637888.1:c.198+8650_198+8652delinsTCA ENSP00000490546.1:n.198+8650_198+8652delinsTCA
ENST00000638076.1:c.*146-127_*146-125delinsTCA ENSP00000490373.1:n.*146-127_*146-125delinsTCA
ENST00000638144.1:n.186-127_186-125delinsTCA
ENST00000646164.1:c.38+8650_38+8652delinsTCA
ENST00000249806.9:c.543-127_543-125delinsTCA ENSP00000249806.5:n.543-127_543-125delinsTCA
ENST00000538696.5:c.639-127_639-125delinsTCA ENSP00000445770.1:n.639-127_639-125delinsTCA
ENST00000562767.1:c.84-12258_84-12256delinsTCA ENSP00000456336.1:n.84-12258_84-12256delinsTCA
ENST00000563917.1:n.443-127_443-125delinsTCA
ENST00000564752.1:c.569-127_569-125delinsTCA ENSP00000457822.1:n.569-127_569-125delinsTCA
ENST00000565471.5:c.84-127_84-125delinsTCA ENSP00000457384.1:n.84-127_84-125delinsTCA
ENST00000566347.5:c.354-127_354-125delinsTCA ENSP00000457783.1:n.354-127_354-125delinsTCA
ENST00000567060.5:c.298-166_298-164delinsTCA ENSP00000454818.1:n.298-166_298-164delinsTCA
NM_017882.2:c.543-127_543-125delinsTCA NP_060352.1:n.543-127_543-125delinsTCA
XR_931861.1:n.765-127_765-125delinsTCA
NM_017882.3:c.543-127_543-125delinsTCA MANE Select NP_060352.1:n.543-127_543-125delinsTCA