Canonical Allele Identifier: CA372805254
Gene: GLIS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.3856016A>C , CM000671.2:g.3856016A>C GRCh38
NC_000009.11:g.3856016A>C , CM000671.1:g.3856016A>C GRCh37
NC_000009.10:g.3846016A>C NCBI36
NG_011782.1:g.449020T>G
NG_011782.2:g.449020T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000464391.2:n.1024T>G
ENST00000491889.6:c.*1829T>G ENSP00000419914.1:n.*1829T>G
ENST00000645252.2:n.908T>G
ENST00000682749.1:c.2001T>G ENSP00000507306.1:p.His667Gln
ENST00000682846.1:c.132-26524T>G ENSP00000507527.1:n.132-26524T>G
ENST00000682864.1:n.965T>G
ENST00000381971.8:c.2466T>G MANE Select ENSP00000371398.3:p.His822Gln
ENST00000645252.1:n.908T>G
ENST00000324333.14:c.2001T>G ENSP00000325494.10:p.His667Gln
ENST00000381971.7:c.2466T>G ENSP00000371398.3:p.His822Gln
ENST00000461870.5:n.822T>G
ENST00000467497.6:n.1006T>G
NM_001042413.1:c.2466T>G NP_001035878.1:p.His822Gln
NM_152629.3:c.2001T>G NP_689842.3:p.His667Gln
XM_005251386.3:c.2001T>G XP_005251443.1:p.His667Gln
XM_005251387.3:c.1800T>G XP_005251444.1:p.His600Gln
XM_005251388.3:c.1800T>G XP_005251445.1:p.His600Gln
XM_011517763.1:c.2466T>G XP_011516065.1:p.His822Gln
XM_011517764.1:c.2466T>G XP_011516066.1:p.His822Gln
XM_011517765.1:c.2466T>G XP_011516067.1:p.His822Gln
XM_011517766.1:c.2001T>G XP_011516068.1:p.His667Gln
XM_011517767.1:c.1800T>G XP_011516069.1:p.His600Gln
XM_005251386.4:c.2001T>G XP_005251443.1:p.His667Gln
XM_005251387.4:c.1800T>G XP_005251444.1:p.His600Gln
XM_005251388.4:c.1800T>G XP_005251445.1:p.His600Gln
XM_011517763.2:c.2466T>G XP_011516065.1:p.His822Gln
XM_011517764.2:c.2466T>G XP_011516066.1:p.His822Gln
XM_011517765.2:c.2466T>G XP_011516067.1:p.His822Gln
XM_011517766.2:c.2001T>G XP_011516068.1:p.His667Gln
XM_011517767.3:c.1800T>G XP_011516069.1:p.His600Gln
XM_017014361.1:c.2001T>G XP_016869850.1:p.His667Gln
NM_001042413.2:c.2466T>G MANE Select NP_001035878.1:p.His822Gln
NM_152629.4:c.2001T>G NP_689842.3:p.His667Gln