Canonical Allele Identifier: CA2518428495
Gene: GLIS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4117703_4117704del , CM000671.2:g.4117703_4117704del GRCh38
NC_000009.11:g.4117703_4117704del , CM000671.1:g.4117703_4117704del GRCh37
NC_000009.10:g.4107703_4107704del NCBI36
NG_011782.1:g.187336_187337del
NG_011782.2:g.187336_187337del

Transcript Alleles

HGVS Amino-acid change
ENST00000491889.6:c.*1073+68_*1073+69del ENSP00000419914.1:n.*1073+68_*1073+69del
ENST00000645252.2:n.152+33240_152+33241del
ENST00000682749.1:c.1245+68_1245+69del ENSP00000507306.1:n.1245+68_1245+69del
ENST00000682846.1:c.131+8034_131+8035del ENSP00000507527.1:n.131+8034_131+8035del
ENST00000381971.8:c.1710+68_1710+69del MANE Select ENSP00000371398.3:n.1710+68_1710+69del
ENST00000645252.1:n.152+33240_152+33241del
ENST00000324333.14:c.1245+68_1245+69del ENSP00000325494.10:n.1245+68_1245+69del
ENST00000381971.7:c.1710+68_1710+69del ENSP00000371398.3:n.1710+68_1710+69del
ENST00000467497.6:n.250+68_250+69del
NM_001042413.1:c.1710+68_1710+69del NP_001035878.1:n.1710+68_1710+69del
NM_152629.3:c.1245+68_1245+69del NP_689842.3:n.1245+68_1245+69del
XM_005251386.3:c.1245+68_1245+69del XP_005251443.1:n.1245+68_1245+69del
XM_005251387.3:c.1044+68_1044+69del XP_005251444.1:n.1044+68_1044+69del
XM_005251388.3:c.1044+68_1044+69del XP_005251445.1:n.1044+68_1044+69del
XM_005251389.3:c.1710+68_1710+69del XP_005251446.1:n.1710+68_1710+69del
XM_006716731.2:c.1710+68_1710+69del XP_006716794.1:n.1710+68_1710+69del
XM_011517763.1:c.1710+68_1710+69del XP_011516065.1:n.1710+68_1710+69del
XM_011517764.1:c.1710+68_1710+69del XP_011516066.1:n.1710+68_1710+69del
XM_011517765.1:c.1710+68_1710+69del XP_011516067.1:n.1710+68_1710+69del
XM_011517766.1:c.1245+68_1245+69del XP_011516068.1:n.1245+68_1245+69del
XM_011517767.1:c.1044+68_1044+69del XP_011516069.1:n.1044+68_1044+69del
XM_011517768.1:c.1710+68_1710+69del XP_011516070.1:n.1710+68_1710+69del
XM_011517769.1:c.1710+68_1710+69del XP_011516071.1:n.1710+68_1710+69del
XR_929206.1:n.2476+68_2476+69del
XM_005251386.4:c.1245+68_1245+69del XP_005251443.1:n.1245+68_1245+69del
XM_005251387.4:c.1044+68_1044+69del XP_005251444.1:n.1044+68_1044+69del
XM_005251388.4:c.1044+68_1044+69del XP_005251445.1:n.1044+68_1044+69del
XM_005251389.5:c.1710+68_1710+69del XP_005251446.1:n.1710+68_1710+69del
XM_006716731.3:c.1710+68_1710+69del XP_006716794.1:n.1710+68_1710+69del
XM_011517763.2:c.1710+68_1710+69del XP_011516065.1:n.1710+68_1710+69del
XM_011517764.2:c.1710+68_1710+69del XP_011516066.1:n.1710+68_1710+69del
XM_011517765.2:c.1710+68_1710+69del XP_011516067.1:n.1710+68_1710+69del
XM_011517766.2:c.1245+68_1245+69del XP_011516068.1:n.1245+68_1245+69del
XM_011517767.3:c.1044+68_1044+69del XP_011516069.1:n.1044+68_1044+69del
XM_011517769.2:c.1710+68_1710+69del XP_011516071.1:n.1710+68_1710+69del
XM_017014361.1:c.1245+68_1245+69del XP_016869850.1:n.1245+68_1245+69del
XR_929206.2:n.2472+68_2472+69del
NM_001042413.2:c.1710+68_1710+69del MANE Select NP_001035878.1:n.1710+68_1710+69del
NM_152629.4:c.1245+68_1245+69del NP_689842.3:n.1245+68_1245+69del