Canonical Allele Identifier: CA2573151123
Gene: CLN6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1400355
ClinVar RCV Id: RCV001932695
dbSNP Id: rs2141145071

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68218584_68218585insAGGAT , CM000677.2:g.68218584_68218585insAGGAT GRCh38
NC_000015.9:g.68510922_68510923insAGGAT , CM000677.1:g.68510922_68510923insAGGAT GRCh37
NC_000015.8:g.66297976_66297977insAGGAT NCBI36
NG_008764.2:g.43627_43628insATCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000249806.11:c.149_150insATCCT MANE Select ENSP00000249806.5:p.Tyr50Ter
ENST00000562767.2:c.83+10917_83+10918insATCCT ENSP00000456336.1:n.83+10917_83+10918insATCCT
ENST00000563917.2:n.41-4197_41-4196insATCCT
ENST00000565471.6:c.84-8826_84-8825insATCCT ENSP00000457384.1:n.84-8826_84-8825insATCCT
ENST00000569336.2:n.58_59insATCCT
ENST00000635747.1:c.*52_*53insATCCT ENSP00000490627.1:n.*52_*53insATCCT
ENST00000636020.1:n.281_282insATCCT
ENST00000636212.1:c.149_150insATCCT ENSP00000489851.1:p.Tyr50Ter
ENST00000636314.1:c.84-4197_84-4196insATCCT ENSP00000490295.1:n.84-4197_84-4196insATCCT
ENST00000636876.1:c.*169_*170insATCCT ENSP00000489950.1:n.*169_*170insATCCT
ENST00000637054.1:c.149_150insATCCT ENSP00000490807.1:p.Tyr50Ter
ENST00000637223.1:c.*52_*53insATCCT ENSP00000490010.1:n.*52_*53insATCCT
ENST00000637329.1:c.60_61insATCCT
ENST00000637450.1:c.84-4197_84-4196insATCCT ENSP00000490204.1:n.84-4197_84-4196insATCCT
ENST00000637494.1:c.149_150insATCCT ENSP00000490057.1:p.Tyr50Ter
ENST00000637667.1:c.149_150insATCCT ENSP00000489843.1:p.Tyr50Ter
ENST00000637823.1:c.75_76insATCCT
ENST00000637888.1:c.149_150insATCCT ENSP00000490546.1:p.Tyr50Ter
ENST00000638076.1:c.149_150insATCCT ENSP00000490373.1:p.Tyr50Ter
ENST00000638144.1:n.31-4197_31-4196insATCCT
ENST00000249806.9:c.149_150insATCCT ENSP00000249806.5:p.Tyr50Ter
ENST00000538696.5:c.245_246insATCCT ENSP00000445770.1:p.Tyr82Ter
ENST00000562767.1:c.83+10917_83+10918insATCCT ENSP00000456336.1:n.83+10917_83+10918insATCCT
ENST00000564752.1:c.149_150insATCCT ENSP00000457822.1:p.Tyr50Ter
ENST00000564846.1:n.581_582insATCCT
ENST00000565471.5:c.84-8826_84-8825insATCCT ENSP00000457384.1:n.84-8826_84-8825insATCCT
ENST00000566347.5:c.149_150insATCCT ENSP00000457783.1:p.Tyr50Ter
ENST00000567060.5:c.149_150insATCCT ENSP00000454818.1:p.Tyr50Ter
ENST00000569336.1:n.235_236insATCCT
NM_017882.2:c.149_150insATCCT NP_060352.1:p.Tyr50Ter
XR_931861.1:n.252_253insATCCT
NM_017882.3:c.149_150insATCCT MANE Select NP_060352.1:p.Tyr50Ter