Canonical Allele Identifier: CA1702647785

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972433_41972437delinsAGTCG , CM000669.2:g.41972433_41972437delinsAGTCG	GRCh38
NC_000007.13:g.42012032_42012036delinsAGTCG , CM000669.1:g.42012032_42012036delinsAGTCG	GRCh37
NC_000007.12:g.41978557_41978561delinsAGTCG	NCBI36
NG_008434.1:g.269583_269587delinsCGACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.2003_2007delinsCGACT MANE Select	ENSP00000379258.3:p.Pro668=
ENST00000677288.1:c.1829_1833delinsCGACT	ENSP00000503986.1:p.Pro610=
ENST00000677605.1:c.2003_2007delinsCGACT	ENSP00000503743.1:p.Pro668=
ENST00000678429.1:c.2003_2007delinsCGACT	ENSP00000502957.1:p.Pro668=
ENST00000395925.7:c.2003_2007delinsCGACT	ENSP00000379258.3:p.Pro668=
ENST00000479210.1:n.1980_1984delinsCGACT
NM_000168.5:c.2003_2007delinsCGACT	NP_000159.3:p.Pro668=
XM_005249703.1:c.2003_2007delinsCGACT	XP_005249760.1:p.Pro668=
XM_005249704.2:c.2003_2007delinsCGACT	XP_005249761.1:p.Pro668=
XM_011515272.1:c.2003_2007delinsCGACT	XP_011513574.1:p.Pro668=
XM_011515273.1:c.2003_2007delinsCGACT	XP_011513575.1:p.Pro668=
XM_011515274.1:c.1826_1830delinsCGACT	XP_011513576.1:p.Pro609=
XM_011515274.2:c.1826_1830delinsCGACT	XP_011513576.1:p.Pro609=
XM_017011997.1:c.2000_2004delinsCGACT	XP_016867486.1:p.Pro667=
NM_000168.6:c.2003_2007delinsCGACT MANE Select	NP_000159.3:p.Pro668=