Canonical Allele Identifier: CA367314894
Community Standard Title: NM_000168.6(GLI3):c.4498G>T (p.Glu1500Ter)
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41964575C>A , CM000669.2:g.41964575C>A GRCh38
NC_000007.13:g.42004173C>A , CM000669.1:g.42004173C>A GRCh37
NC_000007.12:g.41970698C>A NCBI36
NG_008434.1:g.277446G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000168.6:c.4498G>T MANE Select NP_000159.3:p.Glu1500Ter
ENST00000395925.8:c.4498G>T MANE Select ENSP00000379258.3:p.Glu1500Ter
NM_000168.5:c.4498G>T NP_000159.3:p.Glu1500Ter
ENST00000395925.7:c.4498G>T ENSP00000379258.3:p.Glu1500Ter
ENST00000479210.1:n.4475G>T
ENST00000677288.1:c.4324G>T ENSP00000503986.1:p.Glu1442Ter
ENST00000677605.1:c.4498G>T ENSP00000503743.1:p.Glu1500Ter
ENST00000678429.1:c.4498G>T ENSP00000502957.1:p.Glu1500Ter
XM_005249703.1:c.4498G>T XP_005249760.1:p.Glu1500Ter
XM_005249704.2:c.4498G>T XP_005249761.1:p.Glu1500Ter
XM_011515272.1:c.4498G>T XP_011513574.1:p.Glu1500Ter
XM_011515273.1:c.4498G>T XP_011513575.1:p.Glu1500Ter
XM_011515274.1:c.4321G>T XP_011513576.1:p.Glu1441Ter
XM_011515274.2:c.4321G>T XP_011513576.1:p.Glu1441Ter
XM_017011997.1:c.4495G>T XP_016867486.1:p.Glu1499Ter