Canonical Allele Identifier: CA586168815

Gene: GLIS3

Linked Data

• dbSNP Id: rs1193465953
• gnomAD v2: 9-4117664-C-CCT
• gnomAD v3: 9-4117664-C-CCT
• gnomAD v4: 9-4117664-C-CCT
• MyVariant Identifiers: chr9:g.4117664_4117665insCT (hg19) ; chr9:g.4117664_4117665insCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.4117665_4117666insTC , CM000671.2:g.4117665_4117666insTC	GRCh38
NC_000009.11:g.4117665_4117666insTC , CM000671.1:g.4117665_4117666insTC	GRCh37
NC_000009.10:g.4107665_4107666insTC	NCBI36
NG_011782.1:g.187371_187372insAG
NG_011782.2:g.187371_187372insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491889.6:c.*1073+103_*1073+104insAG	ENSP00000419914.1:n.*1073+103_*1073+104insAG
ENST00000645252.2:n.152+33275_152+33276insAG
ENST00000682749.1:c.1245+103_1245+104insAG	ENSP00000507306.1:n.1245+103_1245+104insAG
ENST00000682846.1:c.131+8069_131+8070insAG	ENSP00000507527.1:n.131+8069_131+8070insAG
ENST00000381971.8:c.1710+103_1710+104insAG MANE Select	ENSP00000371398.3:n.1710+103_1710+104insAG
ENST00000645252.1:n.152+33275_152+33276insAG
ENST00000324333.14:c.1245+103_1245+104insAG	ENSP00000325494.10:n.1245+103_1245+104insAG
ENST00000381971.7:c.1710+103_1710+104insAG	ENSP00000371398.3:n.1710+103_1710+104insAG
ENST00000467497.6:n.250+103_250+104insAG
NM_001042413.1:c.1710+103_1710+104insAG	NP_001035878.1:n.1710+103_1710+104insAG
NM_152629.3:c.1245+103_1245+104insAG	NP_689842.3:n.1245+103_1245+104insAG
XM_005251386.3:c.1245+103_1245+104insAG	XP_005251443.1:n.1245+103_1245+104insAG
XM_005251387.3:c.1044+103_1044+104insAG	XP_005251444.1:n.1044+103_1044+104insAG
XM_005251388.3:c.1044+103_1044+104insAG	XP_005251445.1:n.1044+103_1044+104insAG
XM_005251389.3:c.1710+103_1710+104insAG	XP_005251446.1:n.1710+103_1710+104insAG
XM_006716731.2:c.1710+103_1710+104insAG	XP_006716794.1:n.1710+103_1710+104insAG
XM_011517763.1:c.1710+103_1710+104insAG	XP_011516065.1:n.1710+103_1710+104insAG
XM_011517764.1:c.1710+103_1710+104insAG	XP_011516066.1:n.1710+103_1710+104insAG
XM_011517765.1:c.1710+103_1710+104insAG	XP_011516067.1:n.1710+103_1710+104insAG
XM_011517766.1:c.1245+103_1245+104insAG	XP_011516068.1:n.1245+103_1245+104insAG
XM_011517767.1:c.1044+103_1044+104insAG	XP_011516069.1:n.1044+103_1044+104insAG
XM_011517768.1:c.1710+103_1710+104insAG	XP_011516070.1:n.1710+103_1710+104insAG
XM_011517769.1:c.1710+103_1710+104insAG	XP_011516071.1:n.1710+103_1710+104insAG
XR_929206.1:n.2476+103_2476+104insAG
XM_005251386.4:c.1245+103_1245+104insAG	XP_005251443.1:n.1245+103_1245+104insAG
XM_005251387.4:c.1044+103_1044+104insAG	XP_005251444.1:n.1044+103_1044+104insAG
XM_005251388.4:c.1044+103_1044+104insAG	XP_005251445.1:n.1044+103_1044+104insAG
XM_005251389.5:c.1710+103_1710+104insAG	XP_005251446.1:n.1710+103_1710+104insAG
XM_006716731.3:c.1710+103_1710+104insAG	XP_006716794.1:n.1710+103_1710+104insAG
XM_011517763.2:c.1710+103_1710+104insAG	XP_011516065.1:n.1710+103_1710+104insAG
XM_011517764.2:c.1710+103_1710+104insAG	XP_011516066.1:n.1710+103_1710+104insAG
XM_011517765.2:c.1710+103_1710+104insAG	XP_011516067.1:n.1710+103_1710+104insAG
XM_011517766.2:c.1245+103_1245+104insAG	XP_011516068.1:n.1245+103_1245+104insAG
XM_011517767.3:c.1044+103_1044+104insAG	XP_011516069.1:n.1044+103_1044+104insAG
XM_011517769.2:c.1710+103_1710+104insAG	XP_011516071.1:n.1710+103_1710+104insAG
XM_017014361.1:c.1245+103_1245+104insAG	XP_016869850.1:n.1245+103_1245+104insAG
XR_929206.2:n.2472+103_2472+104insAG
NM_001042413.2:c.1710+103_1710+104insAG MANE Select	NP_001035878.1:n.1710+103_1710+104insAG
NM_152629.4:c.1245+103_1245+104insAG	NP_689842.3:n.1245+103_1245+104insAG