Canonical Allele Identifier: CA272384774

Gene: CLN6

Linked Data

• dbSNP Id: rs935340832
• gnomAD v3: 15-68211934-CCT-C
• gnomAD v4: 15-68211934-CCT-C
• MyVariant Identifiers: chr15:g.68504273_68504274del (hg19) ; chr15:g.68211935_68211936del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211936_68211937del , CM000677.2:g.68211936_68211937del	GRCh38
NC_000015.9:g.68504274_68504275del , CM000677.1:g.68504274_68504275del	GRCh37
NC_000015.8:g.66291328_66291329del	NCBI36
NG_008764.2:g.50276_50277del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.298-73_298-72del MANE Select	ENSP00000249806.5:n.298-73_298-72del
ENST00000562767.2:c.84-14308_84-14307del	ENSP00000456336.1:n.84-14308_84-14307del
ENST00000563917.2:n.140-73_140-72del
ENST00000565471.6:c.84-2177_84-2176del	ENSP00000457384.1:n.84-2177_84-2176del
ENST00000635747.1:c.*201-73_*201-72del	ENSP00000490627.1:n.*201-73_*201-72del
ENST00000636212.1:c.298-195_298-194del	ENSP00000489851.1:n.298-195_298-194del
ENST00000636314.1:c.183-618_183-617del	ENSP00000490295.1:n.183-618_183-617del
ENST00000636674.1:n.1208_1209del
ENST00000636964.1:n.1397_1398del
ENST00000637054.1:c.198+6600_198+6601del	ENSP00000490807.1:n.198+6600_198+6601del
ENST00000637223.1:c.*201-618_*201-617del	ENSP00000490010.1:n.*201-618_*201-617del
ENST00000637329.1:c.209-15_209-14del
ENST00000637450.1:c.183-73_183-72del	ENSP00000490204.1:n.183-73_183-72del
ENST00000637494.1:c.199-618_199-617del	ENSP00000490057.1:n.199-618_199-617del
ENST00000637667.1:c.199-73_199-72del	ENSP00000489843.1:n.199-73_199-72del
ENST00000637823.1:c.224-293_224-292del
ENST00000637888.1:c.198+6600_198+6601del	ENSP00000490546.1:n.198+6600_198+6601del
ENST00000638076.1:c.298-73_298-72del	ENSP00000490373.1:n.298-73_298-72del
ENST00000638144.1:n.130-618_130-617del
ENST00000646164.1:c.38+6600_38+6601del
ENST00000249806.9:c.298-73_298-72del	ENSP00000249806.5:n.298-73_298-72del
ENST00000538696.5:c.394-73_394-72del	ENSP00000445770.1:n.394-73_394-72del
ENST00000562767.1:c.84-14308_84-14307del	ENSP00000456336.1:n.84-14308_84-14307del
ENST00000563917.1:n.79-73_79-72del
ENST00000564752.1:c.298-73_298-72del	ENSP00000457822.1:n.298-73_298-72del
ENST00000565471.5:c.84-2177_84-2176del	ENSP00000457384.1:n.84-2177_84-2176del
ENST00000566347.5:c.298-618_298-617del	ENSP00000457783.1:n.298-618_298-617del
ENST00000567060.5:c.298-2216_298-2215del	ENSP00000454818.1:n.298-2216_298-2215del
NM_017882.2:c.298-73_298-72del	NP_060352.1:n.298-73_298-72del
XR_931861.1:n.401-73_401-72del
NM_017882.3:c.298-73_298-72del MANE Select	NP_060352.1:n.298-73_298-72del