Canonical Allele Identifier: CA188327010
Gene: GLIS3 HGNC NCBI

Linked Data

dbSNP Id: rs758230445
gnomAD v4: 9-4117804-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4117804C>G , CM000671.2:g.4117804C>G GRCh38
NC_000009.11:g.4117804C>G , CM000671.1:g.4117804C>G GRCh37
NC_000009.10:g.4107804C>G NCBI36
NG_011782.1:g.187232G>C
NG_011782.2:g.187232G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000491889.6:c.*1037G>C ENSP00000419914.1:n.*1037G>C
ENST00000645252.2:n.152+33136G>C
ENST00000682749.1:c.1209G>C ENSP00000507306.1:p.Met403Ile
ENST00000682846.1:c.131+7930G>C ENSP00000507527.1:n.131+7930G>C
ENST00000381971.8:c.1674G>C MANE Select ENSP00000371398.3:p.Met558Ile
ENST00000645252.1:n.152+33136G>C
ENST00000324333.14:c.1209G>C ENSP00000325494.10:p.Met403Ile
ENST00000381971.7:c.1674G>C ENSP00000371398.3:p.Met558Ile
ENST00000467497.6:n.214G>C
NM_001042413.1:c.1674G>C NP_001035878.1:p.Met558Ile
NM_152629.3:c.1209G>C NP_689842.3:p.Met403Ile
XM_005251386.3:c.1209G>C XP_005251443.1:p.Met403Ile
XM_005251387.3:c.1008G>C XP_005251444.1:p.Met336Ile
XM_005251388.3:c.1008G>C XP_005251445.1:p.Met336Ile
XM_005251389.3:c.1674G>C XP_005251446.1:p.Met558Ile
XM_006716731.2:c.1674G>C XP_006716794.1:p.Met558Ile
XM_011517763.1:c.1674G>C XP_011516065.1:p.Met558Ile
XM_011517764.1:c.1674G>C XP_011516066.1:p.Met558Ile
XM_011517765.1:c.1674G>C XP_011516067.1:p.Met558Ile
XM_011517766.1:c.1209G>C XP_011516068.1:p.Met403Ile
XM_011517767.1:c.1008G>C XP_011516069.1:p.Met336Ile
XM_011517768.1:c.1674G>C XP_011516070.1:p.Met558Ile
XM_011517769.1:c.1674G>C XP_011516071.1:p.Met558Ile
XR_929206.1:n.2440G>C
XM_005251386.4:c.1209G>C XP_005251443.1:p.Met403Ile
XM_005251387.4:c.1008G>C XP_005251444.1:p.Met336Ile
XM_005251388.4:c.1008G>C XP_005251445.1:p.Met336Ile
XM_005251389.5:c.1674G>C XP_005251446.1:p.Met558Ile
XM_006716731.3:c.1674G>C XP_006716794.1:p.Met558Ile
XM_011517763.2:c.1674G>C XP_011516065.1:p.Met558Ile
XM_011517764.2:c.1674G>C XP_011516066.1:p.Met558Ile
XM_011517765.2:c.1674G>C XP_011516067.1:p.Met558Ile
XM_011517766.2:c.1209G>C XP_011516068.1:p.Met403Ile
XM_011517767.3:c.1008G>C XP_011516069.1:p.Met336Ile
XM_011517769.2:c.1674G>C XP_011516071.1:p.Met558Ile
XM_017014361.1:c.1209G>C XP_016869850.1:p.Met403Ile
XR_929206.2:n.2436G>C
NM_001042413.2:c.1674G>C MANE Select NP_001035878.1:p.Met558Ile
NM_152629.4:c.1209G>C NP_689842.3:p.Met403Ile