Canonical Allele Identifier: CA1828933267

Gene: GLIS3

Linked Data

• dbSNP Id: rs1819775652
• gnomAD v4: 9-3856153-TGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.3856157_3856159del , CM000671.2:g.3856157_3856159del	GRCh38
NC_000009.11:g.3856157_3856159del , CM000671.1:g.3856157_3856159del	GRCh37
NC_000009.10:g.3846157_3846159del	NCBI36
NG_011782.1:g.448880_448882del
NG_011782.2:g.448880_448882del

Transcript Alleles

HGVS	Amino-acid change
ENST00000464391.2:n.884_886del
ENST00000491889.6:c.*1689_*1691del	ENSP00000419914.1:n.*1689_*1691del
ENST00000645252.2:n.768_770del
ENST00000682749.1:c.1861_1863del	ENSP00000507306.1:p.His621del
ENST00000682846.1:c.132-26664_132-26662del	ENSP00000507527.1:n.132-26664_132-26662de...
ENST00000682864.1:n.825_827del
ENST00000381971.8:c.2326_2328del MANE Select	ENSP00000371398.3:p.His776del
ENST00000645252.1:n.768_770del
ENST00000324333.14:c.1861_1863del	ENSP00000325494.10:p.His621del
ENST00000381971.7:c.2326_2328del	ENSP00000371398.3:p.His776del
ENST00000461870.5:n.682_684del
ENST00000467497.6:n.866_868del
NM_001042413.1:c.2326_2328del	NP_001035878.1:p.His776del
NM_152629.3:c.1861_1863del	NP_689842.3:p.His621del
XM_005251386.3:c.1861_1863del	XP_005251443.1:p.His621del
XM_005251387.3:c.1660_1662del	XP_005251444.1:p.His554del
XM_005251388.3:c.1660_1662del	XP_005251445.1:p.His554del
XM_011517763.1:c.2326_2328del	XP_011516065.1:p.His776del
XM_011517764.1:c.2326_2328del	XP_011516066.1:p.His776del
XM_011517765.1:c.2326_2328del	XP_011516067.1:p.His776del
XM_011517766.1:c.1861_1863del	XP_011516068.1:p.His621del
XM_011517767.1:c.1660_1662del	XP_011516069.1:p.His554del
XM_005251386.4:c.1861_1863del	XP_005251443.1:p.His621del
XM_005251387.4:c.1660_1662del	XP_005251444.1:p.His554del
XM_005251388.4:c.1660_1662del	XP_005251445.1:p.His554del
XM_011517763.2:c.2326_2328del	XP_011516065.1:p.His776del
XM_011517764.2:c.2326_2328del	XP_011516066.1:p.His776del
XM_011517765.2:c.2326_2328del	XP_011516067.1:p.His776del
XM_011517766.2:c.1861_1863del	XP_011516068.1:p.His621del
XM_011517767.3:c.1660_1662del	XP_011516069.1:p.His554del
XM_017014361.1:c.1861_1863del	XP_016869850.1:p.His621del
NM_001042413.2:c.2326_2328del MANE Select	NP_001035878.1:p.His776del
NM_152629.4:c.1861_1863del	NP_689842.3:p.His621del