Canonical Allele Identifier: CA1702660369

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41964633_41964643delinsAAGTAACTCAG , CM000669.2:g.41964633_41964643delinsAAGTAACTCAG	GRCh38
NC_000007.13:g.42004231_42004241delinsAAGTAACTCAG , CM000669.1:g.42004231_42004241delinsAAGTAACTCAG	GRCh37
NC_000007.12:g.41970756_41970766delinsAAGTAACTCAG	NCBI36
NG_008434.1:g.277378_277388delinsCTGAGTTACTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.4430_4440delinsCTGAGTTACTT MANE Select	ENSP00000379258.3:p.Ser1477=
ENST00000677288.1:c.4256_4266delinsCTGAGTTACTT	ENSP00000503986.1:p.Ser1419=
ENST00000677605.1:c.4430_4440delinsCTGAGTTACTT	ENSP00000503743.1:p.Ser1477=
ENST00000678429.1:c.4430_4440delinsCTGAGTTACTT	ENSP00000502957.1:p.Ser1477=
ENST00000395925.7:c.4430_4440delinsCTGAGTTACTT	ENSP00000379258.3:p.Ser1477=
ENST00000479210.1:n.4407_4417delinsCTGAGTTACTT
NM_000168.5:c.4430_4440delinsCTGAGTTACTT	NP_000159.3:p.Ser1477=
XM_005249703.1:c.4430_4440delinsCTGAGTTACTT	XP_005249760.1:p.Ser1477=
XM_005249704.2:c.4430_4440delinsCTGAGTTACTT	XP_005249761.1:p.Ser1477=
XM_011515272.1:c.4430_4440delinsCTGAGTTACTT	XP_011513574.1:p.Ser1477=
XM_011515273.1:c.4430_4440delinsCTGAGTTACTT	XP_011513575.1:p.Ser1477=
XM_011515274.1:c.4253_4263delinsCTGAGTTACTT	XP_011513576.1:p.Ser1418=
XM_011515274.2:c.4253_4263delinsCTGAGTTACTT	XP_011513576.1:p.Ser1418=
XM_017011997.1:c.4427_4437delinsCTGAGTTACTT	XP_016867486.1:p.Ser1476=
NM_000168.6:c.4430_4440delinsCTGAGTTACTT MANE Select	NP_000159.3:p.Ser1477=