Canonical Allele Identifier: CA1702660130

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41964171_41964172delinsTC , CM000669.2:g.41964171_41964172delinsTC	GRCh38
NC_000007.13:g.42003769_42003770delinsTC , CM000669.1:g.42003769_42003770delinsTC	GRCh37
NC_000007.12:g.41970294_41970295delinsTC	NCBI36
NG_008434.1:g.277849_277850delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.*158_*159delinsGA MANE Select	ENSP00000379258.3:n.*158_*159delinsGA
ENST00000677288.1:c.*158_*159delinsGA	ENSP00000503986.1:n.*158_*159delinsGA
ENST00000677605.1:c.*158_*159delinsGA	ENSP00000503743.1:n.*158_*159delinsGA
ENST00000678429.1:c.*158_*159delinsGA	ENSP00000502957.1:n.*158_*159delinsGA
ENST00000395925.7:c.*158_*159delinsGA	ENSP00000379258.3:n.*158_*159delinsGA
ENST00000479210.1:n.4878_4879delinsGA
NM_000168.5:c.*158_*159delinsGA	NP_000159.3:n.*158_*159delinsGA
XM_005249703.1:c.*158_*159delinsGA	XP_005249760.1:n.*158_*159delinsGA
XM_005249704.2:c.*158_*159delinsGA	XP_005249761.1:n.*158_*159delinsGA
XM_011515272.1:c.*158_*159delinsGA	XP_011513574.1:n.*158_*159delinsGA
XM_011515273.1:c.*158_*159delinsGA	XP_011513575.1:n.*158_*159delinsGA
XM_011515274.1:c.*158_*159delinsGA	XP_011513576.1:n.*158_*159delinsGA
NM_000168.6:c.*158_*159delinsGA MANE Select	NP_000159.3:n.*158_*159delinsGA