Canonical Allele Identifier: CA645567068

Gene: GLI3

Linked Data

• COSMIC: COSM5751769

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42040044_42040045insT , CM000669.2:g.42040044_42040045insT	GRCh38
NC_000007.13:g.42079643_42079644insT , CM000669.1:g.42079643_42079644insT	GRCh37
NC_000007.12:g.42046168_42046169insT	NCBI36
NG_008434.1:g.201975_201976insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1021_1022insA MANE Select	ENSP00000379258.3:p.Ala341AspfsTer?
ENST00000677288.1:c.844_845insA	ENSP00000503986.1:p.Ala282AspfsTer?
ENST00000677605.1:c.1021_1022insA	ENSP00000503743.1:p.Ala341AspfsTer?
ENST00000678429.1:c.1021_1022insA	ENSP00000502957.1:p.Ala341AspfsTer?
ENST00000395925.7:c.1021_1022insA	ENSP00000379258.3:p.Ala341AspfsTer?
ENST00000479210.1:n.998_999insA
NM_000168.5:c.1021_1022insA	NP_000159.3:p.Ala341AspfsTer?
XM_005249703.1:c.1021_1022insA	XP_005249760.1:p.Ala341AspfsTer?
XM_005249704.2:c.1021_1022insA	XP_005249761.1:p.Ala341AspfsTer?
XM_011515272.1:c.1021_1022insA	XP_011513574.1:p.Ala341AspfsTer?
XM_011515273.1:c.1021_1022insA	XP_011513575.1:p.Ala341AspfsTer?
XM_011515274.1:c.844_845insA	XP_011513576.1:p.Ala282AspfsTer?
XM_011515274.2:c.844_845insA	XP_011513576.1:p.Ala282AspfsTer?
XM_017011997.1:c.1018_1019insA	XP_016867486.1:p.Ala340AspfsTer?
NM_000168.6:c.1021_1022insA MANE Select	NP_000159.3:p.Ala341AspfsTer?