Canonical Allele Identifier: CA188287635

Gene: GLIS3

Linked Data

• dbSNP Id: rs1055711777
• gnomAD v2: 9-3856386-TAC-T
• gnomAD v3: 9-3856386-TAC-T
• gnomAD v4: 9-3856386-TAC-T
• MyVariant Identifiers: chr9:g.3856387_3856388del (hg19) ; chr9:g.3856387_3856388del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.3856388_3856389del , CM000671.2:g.3856388_3856389del	GRCh38
NC_000009.11:g.3856388_3856389del , CM000671.1:g.3856388_3856389del	GRCh37
NC_000009.10:g.3846388_3846389del	NCBI36
NG_011782.1:g.448648_448649del
NG_011782.2:g.448648_448649del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464391.2:n.856-204_856-203del
ENST00000491889.6:c.*1661-204_*1661-203del	ENSP00000419914.1:n.*1661-204_*1661-203del
ENST00000645252.2:n.740-204_740-203del
ENST00000682749.1:c.1833-204_1833-203del	ENSP00000507306.1:n.1833-204_1833-203del
ENST00000682846.1:c.132-26896_132-26895del	ENSP00000507527.1:n.132-26896_132-26895del
ENST00000682864.1:n.797-204_797-203del
ENST00000381971.8:c.2298-204_2298-203del MANE Select	ENSP00000371398.3:n.2298-204_2298-203del
ENST00000645252.1:n.740-204_740-203del
ENST00000324333.14:c.1833-204_1833-203del	ENSP00000325494.10:n.1833-204_1833-203del
ENST00000381971.7:c.2298-204_2298-203del	ENSP00000371398.3:n.2298-204_2298-203del
ENST00000461870.5:n.654-204_654-203del
ENST00000467497.6:n.838-204_838-203del
NM_001042413.1:c.2298-204_2298-203del	NP_001035878.1:n.2298-204_2298-203del
NM_152629.3:c.1833-204_1833-203del	NP_689842.3:n.1833-204_1833-203del
XM_005251386.3:c.1833-204_1833-203del	XP_005251443.1:n.1833-204_1833-203del
XM_005251387.3:c.1632-204_1632-203del	XP_005251444.1:n.1632-204_1632-203del
XM_005251388.3:c.1632-204_1632-203del	XP_005251445.1:n.1632-204_1632-203del
XM_011517763.1:c.2298-204_2298-203del	XP_011516065.1:n.2298-204_2298-203del
XM_011517764.1:c.2298-204_2298-203del	XP_011516066.1:n.2298-204_2298-203del
XM_011517765.1:c.2298-204_2298-203del	XP_011516067.1:n.2298-204_2298-203del
XM_011517766.1:c.1833-204_1833-203del	XP_011516068.1:n.1833-204_1833-203del
XM_011517767.1:c.1632-204_1632-203del	XP_011516069.1:n.1632-204_1632-203del
XM_005251386.4:c.1833-204_1833-203del	XP_005251443.1:n.1833-204_1833-203del
XM_005251387.4:c.1632-204_1632-203del	XP_005251444.1:n.1632-204_1632-203del
XM_005251388.4:c.1632-204_1632-203del	XP_005251445.1:n.1632-204_1632-203del
XM_011517763.2:c.2298-204_2298-203del	XP_011516065.1:n.2298-204_2298-203del
XM_011517764.2:c.2298-204_2298-203del	XP_011516066.1:n.2298-204_2298-203del
XM_011517765.2:c.2298-204_2298-203del	XP_011516067.1:n.2298-204_2298-203del
XM_011517766.2:c.1833-204_1833-203del	XP_011516068.1:n.1833-204_1833-203del
XM_011517767.3:c.1632-204_1632-203del	XP_011516069.1:n.1632-204_1632-203del
XM_017014361.1:c.1833-204_1833-203del	XP_016869850.1:n.1833-204_1833-203del
NM_001042413.2:c.2298-204_2298-203del MANE Select	NP_001035878.1:n.2298-204_2298-203del
NM_152629.4:c.1833-204_1833-203del	NP_689842.3:n.1833-204_1833-203del