Canonical Allele Identifier: CA1702660152

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41964208_41964212delinsCAGTT , CM000669.2:g.41964208_41964212delinsCAGTT	GRCh38
NC_000007.13:g.42003806_42003810delinsCAGTT , CM000669.1:g.42003806_42003810delinsCAGTT	GRCh37
NC_000007.12:g.41970331_41970335delinsCAGTT	NCBI36
NG_008434.1:g.277809_277813delinsAACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.*118_*122delinsAACTG MANE Select	ENSP00000379258.3:n.*118_*122delinsAACTG
ENST00000677288.1:c.*118_*122delinsAACTG	ENSP00000503986.1:n.*118_*122delinsAACTG
ENST00000677605.1:c.*118_*122delinsAACTG	ENSP00000503743.1:n.*118_*122delinsAACTG
ENST00000678429.1:c.*118_*122delinsAACTG	ENSP00000502957.1:n.*118_*122delinsAACTG
ENST00000395925.7:c.*118_*122delinsAACTG	ENSP00000379258.3:n.*118_*122delinsAACTG
ENST00000479210.1:n.4838_4842delinsAACTG
NM_000168.5:c.*118_*122delinsAACTG	NP_000159.3:n.*118_*122delinsAACTG
XM_005249703.1:c.*118_*122delinsAACTG	XP_005249760.1:n.*118_*122delinsAACTG
XM_005249704.2:c.*118_*122delinsAACTG	XP_005249761.1:n.*118_*122delinsAACTG
XM_011515272.1:c.*118_*122delinsAACTG	XP_011513574.1:n.*118_*122delinsAACTG
XM_011515273.1:c.*118_*122delinsAACTG	XP_011513575.1:n.*118_*122delinsAACTG
XM_011515274.1:c.*118_*122delinsAACTG	XP_011513576.1:n.*118_*122delinsAACTG
NM_000168.6:c.*118_*122delinsAACTG MANE Select	NP_000159.3:n.*118_*122delinsAACTG