Canonical Allele Identifier: CA2804592649

Gene: CLN6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68209931_68209932insAGA , CM000677.2:g.68209931_68209932insAGA	GRCh38
NC_000015.9:g.68502269_68502270insAGA , CM000677.1:g.68502269_68502270insAGA	GRCh37
NC_000015.8:g.66289323_66289324insAGA	NCBI36
NG_008764.2:g.52280_52281insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249806.11:c.543-173_543-172insTCT MANE Select	ENSP00000249806.5:n.543-173_543-172insTCT
ENST00000562767.2:c.84-12304_84-12303insTCT	ENSP00000456336.1:n.84-12304_84-12303insTCT
ENST00000563917.2:n.385-173_385-172insTCT
ENST00000565471.6:c.84-173_84-172insTCT	ENSP00000457384.1:n.84-173_84-172insTCT
ENST00000635747.1:c.*446-173_*446-172insTCT	ENSP00000490627.1:n.*446-173_*446-172insTCT
ENST00000636212.1:c.*213-173_*213-172insTCT	ENSP00000489851.1:n.*213-173_*213-172insTCT
ENST00000636314.1:c.239-173_239-172insTCT	ENSP00000490295.1:n.239-173_239-172insTCT
ENST00000636674.1:n.1645-173_1645-172insTCT
ENST00000636964.1:n.2071-173_2071-172insTCT
ENST00000637054.1:c.198+8604_198+8605insTCT	ENSP00000490807.1:n.198+8604_198+8605insTCT
ENST00000637223.1:c.*257-173_*257-172insTCT	ENSP00000490010.1:n.*257-173_*257-172insTCT
ENST00000637329.1:c.512-173_512-172insTCT
ENST00000637450.1:c.*197-173_*197-172insTCT	ENSP00000490204.1:n.*197-173_*197-172insTCT
ENST00000637494.1:c.255-173_255-172insTCT	ENSP00000490057.1:n.255-173_255-172insTCT
ENST00000637667.1:c.444-173_444-172insTCT	ENSP00000489843.1:n.444-173_444-172insTCT
ENST00000637823.1:c.368-173_368-172insTCT
ENST00000637888.1:c.198+8604_198+8605insTCT	ENSP00000490546.1:n.198+8604_198+8605insTCT
ENST00000638076.1:c.*146-173_*146-172insTCT	ENSP00000490373.1:n.*146-173_*146-172insTCT
ENST00000638144.1:n.186-173_186-172insTCT
ENST00000646164.1:c.38+8604_38+8605insTCT
ENST00000249806.9:c.543-173_543-172insTCT	ENSP00000249806.5:n.543-173_543-172insTCT
ENST00000538696.5:c.639-173_639-172insTCT	ENSP00000445770.1:n.639-173_639-172insTCT
ENST00000562767.1:c.84-12304_84-12303insTCT	ENSP00000456336.1:n.84-12304_84-12303insTCT
ENST00000563917.1:n.443-173_443-172insTCT
ENST00000564752.1:c.569-173_569-172insTCT	ENSP00000457822.1:n.569-173_569-172insTCT
ENST00000565471.5:c.84-173_84-172insTCT	ENSP00000457384.1:n.84-173_84-172insTCT
ENST00000566347.5:c.354-173_354-172insTCT	ENSP00000457783.1:n.354-173_354-172insTCT
ENST00000567060.5:c.298-212_298-211insTCT	ENSP00000454818.1:n.298-212_298-211insTCT
NM_017882.2:c.543-173_543-172insTCT	NP_060352.1:n.543-173_543-172insTCT
XR_931861.1:n.765-173_765-172insTCT
NM_017882.3:c.543-173_543-172insTCT MANE Select	NP_060352.1:n.543-173_543-172insTCT