Canonical Allele Identifier: CA1702661010

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41965932_41965933delinsCT , CM000669.2:g.41965932_41965933delinsCT	GRCh38
NC_000007.13:g.42005530_42005531delinsCT , CM000669.1:g.42005530_42005531delinsCT	GRCh37
NC_000007.12:g.41972055_41972056delinsCT	NCBI36
NG_008434.1:g.276088_276089delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.3140_3141delinsAG MANE Select	ENSP00000379258.3:p.Gln1047=
ENST00000677288.1:c.2966_2967delinsAG	ENSP00000503986.1:p.Gln989=
ENST00000677605.1:c.3140_3141delinsAG	ENSP00000503743.1:p.Gln1047=
ENST00000678429.1:c.3140_3141delinsAG	ENSP00000502957.1:p.Gln1047=
ENST00000395925.7:c.3140_3141delinsAG	ENSP00000379258.3:p.Gln1047=
ENST00000479210.1:n.3117_3118delinsAG
NM_000168.5:c.3140_3141delinsAG	NP_000159.3:p.Gln1047=
XM_005249703.1:c.3140_3141delinsAG	XP_005249760.1:p.Gln1047=
XM_005249704.2:c.3140_3141delinsAG	XP_005249761.1:p.Gln1047=
XM_011515272.1:c.3140_3141delinsAG	XP_011513574.1:p.Gln1047=
XM_011515273.1:c.3140_3141delinsAG	XP_011513575.1:p.Gln1047=
XM_011515274.1:c.2963_2964delinsAG	XP_011513576.1:p.Gln988=
XM_011515274.2:c.2963_2964delinsAG	XP_011513576.1:p.Gln988=
XM_017011997.1:c.3137_3138delinsAG	XP_016867486.1:p.Gln1046=
NM_000168.6:c.3140_3141delinsAG MANE Select	NP_000159.3:p.Gln1047=