Canonical Allele Identifier: CA372805538
Gene: GLIS3 HGNC NCBI

Linked Data

gnomAD v4: 9-3856154-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.3856154G>T , CM000671.2:g.3856154G>T GRCh38
NC_000009.11:g.3856154G>T , CM000671.1:g.3856154G>T GRCh37
NC_000009.10:g.3846154G>T NCBI36
NG_011782.1:g.448882C>A
NG_011782.2:g.448882C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000464391.2:n.886C>A
ENST00000491889.6:c.*1691C>A ENSP00000419914.1:n.*1691C>A
ENST00000645252.2:n.770C>A
ENST00000682749.1:c.1863C>A ENSP00000507306.1:p.His621Gln
ENST00000682846.1:c.132-26662C>A ENSP00000507527.1:n.132-26662C>A
ENST00000682864.1:n.827C>A
ENST00000381971.8:c.2328C>A MANE Select ENSP00000371398.3:p.His776Gln
ENST00000645252.1:n.770C>A
ENST00000324333.14:c.1863C>A ENSP00000325494.10:p.His621Gln
ENST00000381971.7:c.2328C>A ENSP00000371398.3:p.His776Gln
ENST00000461870.5:n.684C>A
ENST00000467497.6:n.868C>A
NM_001042413.1:c.2328C>A NP_001035878.1:p.His776Gln
NM_152629.3:c.1863C>A NP_689842.3:p.His621Gln
XM_005251386.3:c.1863C>A XP_005251443.1:p.His621Gln
XM_005251387.3:c.1662C>A XP_005251444.1:p.His554Gln
XM_005251388.3:c.1662C>A XP_005251445.1:p.His554Gln
XM_011517763.1:c.2328C>A XP_011516065.1:p.His776Gln
XM_011517764.1:c.2328C>A XP_011516066.1:p.His776Gln
XM_011517765.1:c.2328C>A XP_011516067.1:p.His776Gln
XM_011517766.1:c.1863C>A XP_011516068.1:p.His621Gln
XM_011517767.1:c.1662C>A XP_011516069.1:p.His554Gln
XM_005251386.4:c.1863C>A XP_005251443.1:p.His621Gln
XM_005251387.4:c.1662C>A XP_005251444.1:p.His554Gln
XM_005251388.4:c.1662C>A XP_005251445.1:p.His554Gln
XM_011517763.2:c.2328C>A XP_011516065.1:p.His776Gln
XM_011517764.2:c.2328C>A XP_011516066.1:p.His776Gln
XM_011517765.2:c.2328C>A XP_011516067.1:p.His776Gln
XM_011517766.2:c.1863C>A XP_011516068.1:p.His621Gln
XM_011517767.3:c.1662C>A XP_011516069.1:p.His554Gln
XM_017014361.1:c.1863C>A XP_016869850.1:p.His621Gln
NM_001042413.2:c.2328C>A MANE Select NP_001035878.1:p.His776Gln
NM_152629.4:c.1863C>A NP_689842.3:p.His621Gln