Canonical Allele Identifier: CA1829209830
Gene: GLIS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4292982G= , CM000671.2:g.4292982G= GRCh38
NC_000009.11:g.4292982G= , CM000671.1:g.4292982G= GRCh37
NC_000009.10:g.4282982G= NCBI36
NG_011782.1:g.12054C=
NG_011782.2:g.12054C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000491889.6:c.-99+6439C= ENSP00000419914.1:n.-99+6439C=
ENST00000682749.1:c.-78+6439C= ENSP00000507306.1:n.-78+6439C=
ENST00000381971.8:c.-99+6439C= MANE Select ENSP00000371398.3:n.-99+6439C=
ENST00000381971.7:c.-99+6439C= ENSP00000371398.3:n.-99+6439C=
ENST00000465708.5:n.496+6439C=
ENST00000471664.1:n.585-6459C=
ENST00000477901.5:c.-99+6439C= ENSP00000417794.1:n.-99+6439C=
ENST00000478844.5:c.-78+5402C= ENSP00000418005.1:n.-78+5402C=
ENST00000481827.5:c.-99+5402C= ENSP00000417883.1:n.-99+5402C=
ENST00000490709.1:n.416+6439C=
ENST00000491889.5:c.-99+6439C= ENSP00000419914.1:n.-99+6439C=
NM_001042413.1:c.-99+6439C= NP_001035878.1:n.-99+6439C=
XM_005251386.3:c.-78+6439C= XP_005251443.1:n.-78+6439C=
XM_005251387.3:c.-557+6439C= XP_005251444.1:n.-557+6439C=
XM_005251388.3:c.-71+6439C= XP_005251445.1:n.-71+6439C=
XM_005251389.3:c.-99+6439C= XP_005251446.1:n.-99+6439C=
XM_006716731.2:c.-99+6439C= XP_006716794.1:n.-99+6439C=
XM_011517763.1:c.-98-6459C= XP_011516065.1:n.-98-6459C=
XM_011517764.1:c.-99+5402C= XP_011516066.1:n.-99+5402C=
XM_011517765.1:c.-99+6439C= XP_011516067.1:n.-99+6439C=
XM_011517767.1:c.-557+5402C= XP_011516069.1:n.-557+5402C=
XM_011517768.1:c.-99+6439C= XP_011516070.1:n.-99+6439C=
XM_011517769.1:c.-99+6439C= XP_011516071.1:n.-99+6439C=
XR_929206.1:n.668+6439C=
XM_005251386.4:c.-78+6439C= XP_005251443.1:n.-78+6439C=
XM_005251387.4:c.-557+6439C= XP_005251444.1:n.-557+6439C=
XM_005251388.4:c.-71+6439C= XP_005251445.1:n.-71+6439C=
XM_005251389.5:c.-99+6439C= XP_005251446.1:n.-99+6439C=
XM_006716731.3:c.-99+6439C= XP_006716794.1:n.-99+6439C=
XM_011517763.2:c.-98-6459C= XP_011516065.1:n.-98-6459C=
XM_011517764.2:c.-99+5402C= XP_011516066.1:n.-99+5402C=
XM_011517765.2:c.-99+6439C= XP_011516067.1:n.-99+6439C=
XM_011517767.3:c.-557+5402C= XP_011516069.1:n.-557+5402C=
XM_011517769.2:c.-99+6439C= XP_011516071.1:n.-99+6439C=
XR_929206.2:n.664+6439C=
NM_001042413.2:c.-99+6439C= MANE Select NP_001035878.1:n.-99+6439C=