Canonical Allele Identifier: CA2689273682

Gene: GLIS3

Linked Data

• gnomAD v4: 9-3856158-TGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.3856162_3856164del , CM000671.2:g.3856162_3856164del	GRCh38
NC_000009.11:g.3856162_3856164del , CM000671.1:g.3856162_3856164del	GRCh37
NC_000009.10:g.3846162_3846164del	NCBI36
NG_011782.1:g.448875_448877del
NG_011782.2:g.448875_448877del

Transcript Alleles

HGVS	Amino-acid change
ENST00000464391.2:n.879_881del
ENST00000491889.6:c.*1684_*1686del	ENSP00000419914.1:n.*1684_*1686del
ENST00000645252.2:n.763_765del
ENST00000682749.1:c.1856_1858del	ENSP00000507306.1:p.Pro619del
ENST00000682846.1:c.132-26669_132-26667del	ENSP00000507527.1:n.132-26669_132-26667de...
ENST00000682864.1:n.820_822del
ENST00000381971.8:c.2321_2323del MANE Select	ENSP00000371398.3:p.Pro774del
ENST00000645252.1:n.763_765del
ENST00000324333.14:c.1856_1858del	ENSP00000325494.10:p.Pro619del
ENST00000381971.7:c.2321_2323del	ENSP00000371398.3:p.Pro774del
ENST00000461870.5:n.677_679del
ENST00000467497.6:n.861_863del
NM_001042413.1:c.2321_2323del	NP_001035878.1:p.Pro774del
NM_152629.3:c.1856_1858del	NP_689842.3:p.Pro619del
XM_005251386.3:c.1856_1858del	XP_005251443.1:p.Pro619del
XM_005251387.3:c.1655_1657del	XP_005251444.1:p.Pro552del
XM_005251388.3:c.1655_1657del	XP_005251445.1:p.Pro552del
XM_011517763.1:c.2321_2323del	XP_011516065.1:p.Pro774del
XM_011517764.1:c.2321_2323del	XP_011516066.1:p.Pro774del
XM_011517765.1:c.2321_2323del	XP_011516067.1:p.Pro774del
XM_011517766.1:c.1856_1858del	XP_011516068.1:p.Pro619del
XM_011517767.1:c.1655_1657del	XP_011516069.1:p.Pro552del
XM_005251386.4:c.1856_1858del	XP_005251443.1:p.Pro619del
XM_005251387.4:c.1655_1657del	XP_005251444.1:p.Pro552del
XM_005251388.4:c.1655_1657del	XP_005251445.1:p.Pro552del
XM_011517763.2:c.2321_2323del	XP_011516065.1:p.Pro774del
XM_011517764.2:c.2321_2323del	XP_011516066.1:p.Pro774del
XM_011517765.2:c.2321_2323del	XP_011516067.1:p.Pro774del
XM_011517766.2:c.1856_1858del	XP_011516068.1:p.Pro619del
XM_011517767.3:c.1655_1657del	XP_011516069.1:p.Pro552del
XM_017014361.1:c.1856_1858del	XP_016869850.1:p.Pro619del
NM_001042413.2:c.2321_2323del MANE Select	NP_001035878.1:p.Pro774del
NM_152629.4:c.1856_1858del	NP_689842.3:p.Pro619del