Canonical Allele Identifier: CA1702647778

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972427_41972428delinsTC , CM000669.2:g.41972427_41972428delinsTC	GRCh38
NC_000007.13:g.42012026_42012027delinsTC , CM000669.1:g.42012026_42012027delinsTC	GRCh37
NC_000007.12:g.41978551_41978552delinsTC	NCBI36
NG_008434.1:g.269592_269593delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.2012_2013delinsGA MANE Select	ENSP00000379258.3:p.Gly671=
ENST00000677288.1:c.1838_1839delinsGA	ENSP00000503986.1:p.Gly613=
ENST00000677605.1:c.2012_2013delinsGA	ENSP00000503743.1:p.Gly671=
ENST00000678429.1:c.2012_2013delinsGA	ENSP00000502957.1:p.Gly671=
ENST00000395925.7:c.2012_2013delinsGA	ENSP00000379258.3:p.Gly671=
ENST00000479210.1:n.1989_1990delinsGA
NM_000168.5:c.2012_2013delinsGA	NP_000159.3:p.Gly671=
XM_005249703.1:c.2012_2013delinsGA	XP_005249760.1:p.Gly671=
XM_005249704.2:c.2012_2013delinsGA	XP_005249761.1:p.Gly671=
XM_011515272.1:c.2012_2013delinsGA	XP_011513574.1:p.Gly671=
XM_011515273.1:c.2012_2013delinsGA	XP_011513575.1:p.Gly671=
XM_011515274.1:c.1835_1836delinsGA	XP_011513576.1:p.Gly612=
XM_011515274.2:c.1835_1836delinsGA	XP_011513576.1:p.Gly612=
XM_017011997.1:c.2009_2010delinsGA	XP_016867486.1:p.Gly670=
NM_000168.6:c.2012_2013delinsGA MANE Select	NP_000159.3:p.Gly671=