Canonical Allele Identifier: CA1702659328

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41962569_41962570delinsAG , CM000669.2:g.41962569_41962570delinsAG	GRCh38
NC_000007.13:g.42002167_42002168delinsAG , CM000669.1:g.42002167_42002168delinsAG	GRCh37
NC_000007.12:g.41968692_41968693delinsAG	NCBI36
NG_008434.1:g.279451_279452delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.*1760_*1761delinsCT MANE Select	ENSP00000379258.3:n.*1760_*1761delinsCT
ENST00000677288.1:c.*1760_*1761delinsCT	ENSP00000503986.1:n.*1760_*1761delinsCT
ENST00000677605.1:c.*1760_*1761delinsCT	ENSP00000503743.1:n.*1760_*1761delinsCT
ENST00000678429.1:c.*1760_*1761delinsCT	ENSP00000502957.1:n.*1760_*1761delinsCT
ENST00000395925.7:c.*1760_*1761delinsCT	ENSP00000379258.3:n.*1760_*1761delinsCT
NM_000168.5:c.*1760_*1761delinsCT	NP_000159.3:n.*1760_*1761delinsCT
XM_005249703.1:c.*1760_*1761delinsCT	XP_005249760.1:n.*1760_*1761delinsCT
XM_005249704.2:c.*1760_*1761delinsCT	XP_005249761.1:n.*1760_*1761delinsCT
XM_011515272.1:c.*1760_*1761delinsCT	XP_011513574.1:n.*1760_*1761delinsCT
XM_011515273.1:c.*1760_*1761delinsCT	XP_011513575.1:n.*1760_*1761delinsCT
XM_011515274.1:c.*1760_*1761delinsCT	XP_011513576.1:n.*1760_*1761delinsCT
NM_000168.6:c.*1760_*1761delinsCT MANE Select	NP_000159.3:n.*1760_*1761delinsCT