Canonical Allele Identifier: CA1829088370
Gene: GLIS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4117734_4117736delinsAAG , CM000671.2:g.4117734_4117736delinsAAG GRCh38
NC_000009.11:g.4117734_4117736delinsAAG , CM000671.1:g.4117734_4117736delinsAAG GRCh37
NC_000009.10:g.4107734_4107736delinsAAG NCBI36
NG_011782.1:g.187300_187302delinsCTT
NG_011782.2:g.187300_187302delinsCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000491889.6:c.*1073+32_*1073+34delinsCTT ENSP00000419914.1:n.*1073+32_*1073+34deli...
ENST00000645252.2:n.152+33204_152+33206delinsCTT
ENST00000682749.1:c.1245+32_1245+34delinsCTT ENSP00000507306.1:n.1245+32_1245+34delins...
ENST00000682846.1:c.131+7998_131+8000delinsCTT ENSP00000507527.1:n.131+7998_131+8000deli...
ENST00000381971.8:c.1710+32_1710+34delinsCTT MANE Select ENSP00000371398.3:n.1710+32_1710+34delins...
ENST00000645252.1:n.152+33204_152+33206delinsCTT
ENST00000324333.14:c.1245+32_1245+34delinsCTT ENSP00000325494.10:n.1245+32_1245+34delin...
ENST00000381971.7:c.1710+32_1710+34delinsCTT ENSP00000371398.3:n.1710+32_1710+34delins...
ENST00000467497.6:n.250+32_250+34delinsCTT
NM_001042413.1:c.1710+32_1710+34delinsCTT NP_001035878.1:n.1710+32_1710+34delinsCTT...
NM_152629.3:c.1245+32_1245+34delinsCTT NP_689842.3:n.1245+32_1245+34delinsCTT
XM_005251386.3:c.1245+32_1245+34delinsCTT XP_005251443.1:n.1245+32_1245+34delinsCTT...
XM_005251387.3:c.1044+32_1044+34delinsCTT XP_005251444.1:n.1044+32_1044+34delinsCTT...
XM_005251388.3:c.1044+32_1044+34delinsCTT XP_005251445.1:n.1044+32_1044+34delinsCTT...
XM_005251389.3:c.1710+32_1710+34delinsCTT XP_005251446.1:n.1710+32_1710+34delinsCTT...
XM_006716731.2:c.1710+32_1710+34delinsCTT XP_006716794.1:n.1710+32_1710+34delinsCTT...
XM_011517763.1:c.1710+32_1710+34delinsCTT XP_011516065.1:n.1710+32_1710+34delinsCTT...
XM_011517764.1:c.1710+32_1710+34delinsCTT XP_011516066.1:n.1710+32_1710+34delinsCTT...
XM_011517765.1:c.1710+32_1710+34delinsCTT XP_011516067.1:n.1710+32_1710+34delinsCTT...
XM_011517766.1:c.1245+32_1245+34delinsCTT XP_011516068.1:n.1245+32_1245+34delinsCTT...
XM_011517767.1:c.1044+32_1044+34delinsCTT XP_011516069.1:n.1044+32_1044+34delinsCTT...
XM_011517768.1:c.1710+32_1710+34delinsCTT XP_011516070.1:n.1710+32_1710+34delinsCTT...
XM_011517769.1:c.1710+32_1710+34delinsCTT XP_011516071.1:n.1710+32_1710+34delinsCTT...
XR_929206.1:n.2476+32_2476+34delinsCTT
XM_005251386.4:c.1245+32_1245+34delinsCTT XP_005251443.1:n.1245+32_1245+34delinsCTT...
XM_005251387.4:c.1044+32_1044+34delinsCTT XP_005251444.1:n.1044+32_1044+34delinsCTT...
XM_005251388.4:c.1044+32_1044+34delinsCTT XP_005251445.1:n.1044+32_1044+34delinsCTT...
XM_005251389.5:c.1710+32_1710+34delinsCTT XP_005251446.1:n.1710+32_1710+34delinsCTT...
XM_006716731.3:c.1710+32_1710+34delinsCTT XP_006716794.1:n.1710+32_1710+34delinsCTT...
XM_011517763.2:c.1710+32_1710+34delinsCTT XP_011516065.1:n.1710+32_1710+34delinsCTT...
XM_011517764.2:c.1710+32_1710+34delinsCTT XP_011516066.1:n.1710+32_1710+34delinsCTT...
XM_011517765.2:c.1710+32_1710+34delinsCTT XP_011516067.1:n.1710+32_1710+34delinsCTT...
XM_011517766.2:c.1245+32_1245+34delinsCTT XP_011516068.1:n.1245+32_1245+34delinsCTT...
XM_011517767.3:c.1044+32_1044+34delinsCTT XP_011516069.1:n.1044+32_1044+34delinsCTT...
XM_011517769.2:c.1710+32_1710+34delinsCTT XP_011516071.1:n.1710+32_1710+34delinsCTT...
XM_017014361.1:c.1245+32_1245+34delinsCTT XP_016869850.1:n.1245+32_1245+34delinsCTT...
XR_929206.2:n.2472+32_2472+34delinsCTT
NM_001042413.2:c.1710+32_1710+34delinsCTT MANE Select NP_001035878.1:n.1710+32_1710+34delinsCTT...
NM_152629.4:c.1245+32_1245+34delinsCTT NP_689842.3:n.1245+32_1245+34delinsCTT