Canonical Allele Identifier: CA651329673
Gene: GLI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41963507_41963508insA , CM000669.2:g.41963507_41963508insA GRCh38
NC_000007.13:g.42003105_42003106insA , CM000669.1:g.42003105_42003106insA GRCh37
NC_000007.12:g.41969630_41969631insA NCBI36
NG_008434.1:g.278513_278514insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000395925.8:c.*822_*823insT MANE Select ENSP00000379258.3:n.*822_*823insT
ENST00000677288.1:c.*822_*823insT ENSP00000503986.1:n.*822_*823insT
ENST00000677605.1:c.*822_*823insT ENSP00000503743.1:n.*822_*823insT
ENST00000678429.1:c.*822_*823insT ENSP00000502957.1:n.*822_*823insT
ENST00000395925.7:c.*822_*823insT ENSP00000379258.3:n.*822_*823insT
NM_000168.5:c.*822_*823insT NP_000159.3:n.*822_*823insT
XM_005249703.1:c.*822_*823insT XP_005249760.1:n.*822_*823insT
XM_005249704.2:c.*822_*823insT XP_005249761.1:n.*822_*823insT
XM_011515272.1:c.*822_*823insT XP_011513574.1:n.*822_*823insT
XM_011515273.1:c.*822_*823insT XP_011513575.1:n.*822_*823insT
XM_011515274.1:c.*822_*823insT XP_011513576.1:n.*822_*823insT
NM_000168.6:c.*822_*823insT MANE Select NP_000159.3:n.*822_*823insT