Canonical Allele Identifier: CA586168843
Gene: GLIS3 HGNC NCBI

Linked Data

dbSNP Id: rs1287259480

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4118820_4118834del , CM000671.2:g.4118820_4118834del GRCh38
NC_000009.11:g.4118820_4118834del , CM000671.1:g.4118820_4118834del GRCh37
NC_000009.10:g.4108820_4108834del NCBI36
NG_011782.1:g.186203_186217del
NG_011782.2:g.186203_186217del

Transcript Alleles

HGVS Amino-acid Change
ENST00000491889.6:c.*8_*22del ENSP00000419914.1:n.*8_*22del
ENST00000645252.2:n.152+32107_152+32121del
ENST00000682749.1:c.180_194del ENSP00000507306.1:p.Glu61_Ala65del
ENST00000682846.1:c.131+6901_131+6915del ENSP00000507527.1:n.131+6901_131+6915del
ENST00000381971.8:c.645_659del MANE Select ENSP00000371398.3:p.Glu216_Ala220del
ENST00000645252.1:n.152+32107_152+32121del
ENST00000324333.14:c.180_194del ENSP00000325494.10:p.Glu61_Ala65del
ENST00000381971.7:c.645_659del ENSP00000371398.3:p.Glu216_Ala220del
ENST00000462164.5:c.180_194del ENSP00000418671.1:p.Glu61_Ala65del
ENST00000473846.5:n.404_418del
ENST00000477901.5:c.645_659del ENSP00000417794.1:p.Glu216_Ala220del
ENST00000478315.5:c.180_194del ENSP00000418995.1:p.Glu61_Ala65del
ENST00000478844.5:c.180_194del ENSP00000418005.1:p.Glu61_Ala65del
ENST00000481827.5:c.645_659del ENSP00000417883.1:p.Glu216_Ala220del
ENST00000490709.1:n.465_479del
ENST00000491889.5:c.*8_*22del ENSP00000419914.1:n.*8_*22del
NM_001042413.1:c.645_659del NP_001035878.1:p.Glu216_Ala220del
NM_152629.3:c.180_194del NP_689842.3:p.Glu61_Ala65del
XM_005251386.3:c.180_194del XP_005251443.1:p.Glu61_Ala65del
XM_005251387.3:c.-22_-8del XP_005251444.1:n.-22_-8del
XM_005251388.3:c.-22_-8del XP_005251445.1:n.-22_-8del
XM_005251389.3:c.645_659del XP_005251446.1:p.Glu216_Ala220del
XM_006716731.2:c.645_659del XP_006716794.1:p.Glu216_Ala220del
XM_011517763.1:c.645_659del XP_011516065.1:p.Glu216_Ala220del
XM_011517764.1:c.645_659del XP_011516066.1:p.Glu216_Ala220del
XM_011517765.1:c.645_659del XP_011516067.1:p.Glu216_Ala220del
XM_011517766.1:c.180_194del XP_011516068.1:p.Glu61_Ala65del
XM_011517767.1:c.-22_-8del XP_011516069.1:n.-22_-8del
XM_011517768.1:c.645_659del XP_011516070.1:p.Glu216_Ala220del
XM_011517769.1:c.645_659del XP_011516071.1:p.Glu216_Ala220del
XR_929206.1:n.1411_1425del
XM_005251386.4:c.180_194del XP_005251443.1:p.Glu61_Ala65del
XM_005251387.4:c.-22_-8del XP_005251444.1:n.-22_-8del
XM_005251388.4:c.-22_-8del XP_005251445.1:n.-22_-8del
XM_005251389.5:c.645_659del XP_005251446.1:p.Glu216_Ala220del
XM_006716731.3:c.645_659del XP_006716794.1:p.Glu216_Ala220del
XM_011517763.2:c.645_659del XP_011516065.1:p.Glu216_Ala220del
XM_011517764.2:c.645_659del XP_011516066.1:p.Glu216_Ala220del
XM_011517765.2:c.645_659del XP_011516067.1:p.Glu216_Ala220del
XM_011517766.2:c.180_194del XP_011516068.1:p.Glu61_Ala65del
XM_011517767.3:c.-22_-8del XP_011516069.1:n.-22_-8del
XM_011517769.2:c.645_659del XP_011516071.1:p.Glu216_Ala220del
XM_017014361.1:c.180_194del XP_016869850.1:p.Glu61_Ala65del
XR_929206.2:n.1407_1421del
NM_001042413.2:c.645_659del MANE Select NP_001035878.1:p.Glu216_Ala220del
NM_152629.4:c.180_194del NP_689842.3:p.Glu61_Ala65del