Canonical Allele Identifier: CA15592431
Gene: GLIS3 HGNC NCBI

Linked Data

dbSNP Id: rs10814916

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4293150A>C , CM000671.2:g.4293150A>C GRCh38
NC_000009.11:g.4293150A>C , CM000671.1:g.4293150A>C GRCh37
NC_000009.10:g.4283150A>C NCBI36
NG_011782.1:g.11886T>G
NG_011782.2:g.11886T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000491889.6:c.-99+6271T>G ENSP00000419914.1:p.=
ENST00000682749.1:c.-78+6271T>G ENSP00000507306.1:p.=
ENST00000381971.8:c.-99+6271T>G MANE Select ENSP00000371398.3:p.=
ENST00000381971.7:c.-99+6271T>G ENSP00000371398.3:p.=
ENST00000465708.5:n.496+6271T>G
ENST00000471664.1:n.585-6627T>G
ENST00000477901.5:c.-99+6271T>G ENSP00000417794.1:p.=
ENST00000478844.5:c.-78+5234T>G ENSP00000418005.1:p.=
ENST00000481827.5:c.-99+5234T>G ENSP00000417883.1:p.=
ENST00000490709.1:n.416+6271T>G
ENST00000491889.5:c.-99+6271T>G ENSP00000419914.1:p.=
NM_001042413.1:c.-99+6271T>G NP_001035878.1:p.=
XM_005251386.3:c.-78+6271T>G XP_005251443.1:p.=
XM_005251387.3:c.-557+6271T>G XP_005251444.1:p.=
XM_005251388.3:c.-71+6271T>G XP_005251445.1:p.=
XM_005251389.3:c.-99+6271T>G XP_005251446.1:p.=
XM_006716731.2:c.-99+6271T>G XP_006716794.1:p.=
XM_011517763.1:c.-98-6627T>G XP_011516065.1:p.=
XM_011517764.1:c.-99+5234T>G XP_011516066.1:p.=
XM_011517765.1:c.-99+6271T>G XP_011516067.1:p.=
XM_011517767.1:c.-557+5234T>G XP_011516069.1:p.=
XM_011517768.1:c.-99+6271T>G XP_011516070.1:p.=
XM_011517769.1:c.-99+6271T>G XP_011516071.1:p.=
XR_929206.1:n.668+6271T>G
XM_005251386.4:c.-78+6271T>G XP_005251443.1:p.=
XM_005251387.4:c.-557+6271T>G XP_005251444.1:p.=
XM_005251388.4:c.-71+6271T>G XP_005251445.1:p.=
XM_005251389.5:c.-99+6271T>G XP_005251446.1:p.=
XM_006716731.3:c.-99+6271T>G XP_006716794.1:p.=
XM_011517763.2:c.-98-6627T>G XP_011516065.1:p.=
XM_011517764.2:c.-99+5234T>G XP_011516066.1:p.=
XM_011517765.2:c.-99+6271T>G XP_011516067.1:p.=
XM_011517767.3:c.-557+5234T>G XP_011516069.1:p.=
XM_011517769.2:c.-99+6271T>G XP_011516071.1:p.=
XR_929206.2:n.664+6271T>G
NM_001042413.2:c.-99+6271T>G MANE Select NP_001035878.1:p.=