Canonical Allele Identifier: CA651329643

Gene: GLI3

Linked Data

• COSMIC: COSN23794057

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41962341_41962342insC , CM000669.2:g.41962341_41962342insC	GRCh38
NC_000007.13:g.42001939_42001940insC , CM000669.1:g.42001939_42001940insC	GRCh37
NC_000007.12:g.41968464_41968465insC	NCBI36
NG_008434.1:g.279679_279680insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.*1988_*1989insG MANE Select	ENSP00000379258.3:n.*1988_*1989insG
ENST00000677288.1:c.*1988_*1989insG	ENSP00000503986.1:n.*1988_*1989insG
ENST00000677605.1:c.*1988_*1989insG	ENSP00000503743.1:n.*1988_*1989insG
ENST00000678429.1:c.*1988_*1989insG	ENSP00000502957.1:n.*1988_*1989insG
ENST00000395925.7:c.*1988_*1989insG	ENSP00000379258.3:n.*1988_*1989insG
NM_000168.5:c.*1988_*1989insG	NP_000159.3:n.*1988_*1989insG
XM_005249703.1:c.*1988_*1989insG	XP_005249760.1:n.*1988_*1989insG
XM_005249704.2:c.*1988_*1989insG	XP_005249761.1:n.*1988_*1989insG
XM_011515272.1:c.*1988_*1989insG	XP_011513574.1:n.*1988_*1989insG
XM_011515273.1:c.*1988_*1989insG	XP_011513575.1:n.*1988_*1989insG
XM_011515274.1:c.*1988_*1989insG	XP_011513576.1:n.*1988_*1989insG
NM_000168.6:c.*1988_*1989insG MANE Select	NP_000159.3:n.*1988_*1989insG