Canonical Allele Identifier: CA2555048169

Gene: GLIS3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.4117710_4117711del , CM000671.2:g.4117710_4117711del	GRCh38
NC_000009.11:g.4117710_4117711del , CM000671.1:g.4117710_4117711del	GRCh37
NC_000009.10:g.4107710_4107711del	NCBI36
NG_011782.1:g.187325_187326del
NG_011782.2:g.187325_187326del

Transcript Alleles

HGVS	Amino-acid change
ENST00000491889.6:c.*1073+57_*1073+58del	ENSP00000419914.1:n.*1073+57_*1073+58del
ENST00000645252.2:n.152+33229_152+33230del
ENST00000682749.1:c.1245+57_1245+58del	ENSP00000507306.1:n.1245+57_1245+58del
ENST00000682846.1:c.131+8023_131+8024del	ENSP00000507527.1:n.131+8023_131+8024del
ENST00000381971.8:c.1710+57_1710+58del MANE Select	ENSP00000371398.3:n.1710+57_1710+58del
ENST00000645252.1:n.152+33229_152+33230del
ENST00000324333.14:c.1245+57_1245+58del	ENSP00000325494.10:n.1245+57_1245+58del
ENST00000381971.7:c.1710+57_1710+58del	ENSP00000371398.3:n.1710+57_1710+58del
ENST00000467497.6:n.250+57_250+58del
NM_001042413.1:c.1710+57_1710+58del	NP_001035878.1:n.1710+57_1710+58del
NM_152629.3:c.1245+57_1245+58del	NP_689842.3:n.1245+57_1245+58del
XM_005251386.3:c.1245+57_1245+58del	XP_005251443.1:n.1245+57_1245+58del
XM_005251387.3:c.1044+57_1044+58del	XP_005251444.1:n.1044+57_1044+58del
XM_005251388.3:c.1044+57_1044+58del	XP_005251445.1:n.1044+57_1044+58del
XM_005251389.3:c.1710+57_1710+58del	XP_005251446.1:n.1710+57_1710+58del
XM_006716731.2:c.1710+57_1710+58del	XP_006716794.1:n.1710+57_1710+58del
XM_011517763.1:c.1710+57_1710+58del	XP_011516065.1:n.1710+57_1710+58del
XM_011517764.1:c.1710+57_1710+58del	XP_011516066.1:n.1710+57_1710+58del
XM_011517765.1:c.1710+57_1710+58del	XP_011516067.1:n.1710+57_1710+58del
XM_011517766.1:c.1245+57_1245+58del	XP_011516068.1:n.1245+57_1245+58del
XM_011517767.1:c.1044+57_1044+58del	XP_011516069.1:n.1044+57_1044+58del
XM_011517768.1:c.1710+57_1710+58del	XP_011516070.1:n.1710+57_1710+58del
XM_011517769.1:c.1710+57_1710+58del	XP_011516071.1:n.1710+57_1710+58del
XR_929206.1:n.2476+57_2476+58del
XM_005251386.4:c.1245+57_1245+58del	XP_005251443.1:n.1245+57_1245+58del
XM_005251387.4:c.1044+57_1044+58del	XP_005251444.1:n.1044+57_1044+58del
XM_005251388.4:c.1044+57_1044+58del	XP_005251445.1:n.1044+57_1044+58del
XM_005251389.5:c.1710+57_1710+58del	XP_005251446.1:n.1710+57_1710+58del
XM_006716731.3:c.1710+57_1710+58del	XP_006716794.1:n.1710+57_1710+58del
XM_011517763.2:c.1710+57_1710+58del	XP_011516065.1:n.1710+57_1710+58del
XM_011517764.2:c.1710+57_1710+58del	XP_011516066.1:n.1710+57_1710+58del
XM_011517765.2:c.1710+57_1710+58del	XP_011516067.1:n.1710+57_1710+58del
XM_011517766.2:c.1245+57_1245+58del	XP_011516068.1:n.1245+57_1245+58del
XM_011517767.3:c.1044+57_1044+58del	XP_011516069.1:n.1044+57_1044+58del
XM_011517769.2:c.1710+57_1710+58del	XP_011516071.1:n.1710+57_1710+58del
XM_017014361.1:c.1245+57_1245+58del	XP_016869850.1:n.1245+57_1245+58del
XR_929206.2:n.2472+57_2472+58del
NM_001042413.2:c.1710+57_1710+58del MANE Select	NP_001035878.1:n.1710+57_1710+58del
NM_152629.4:c.1245+57_1245+58del	NP_689842.3:n.1245+57_1245+58del