Canonical Allele Identifier: CA917990717

Gene: GLI3

Linked Data

• dbSNP Id: rs1562655709

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41963387_41963388del , CM000669.2:g.41963387_41963388del	GRCh38
NC_000007.13:g.42002985_42002986del , CM000669.1:g.42002985_42002986del	GRCh37
NC_000007.12:g.41969510_41969511del	NCBI36
NG_008434.1:g.278636_278637del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.*945_*946del MANE Select	ENSP00000379258.3:n.*945_*946del
ENST00000677288.1:c.*945_*946del	ENSP00000503986.1:n.*945_*946del
ENST00000677605.1:c.*945_*946del	ENSP00000503743.1:n.*945_*946del
ENST00000678429.1:c.*945_*946del	ENSP00000502957.1:n.*945_*946del
ENST00000395925.7:c.*945_*946del	ENSP00000379258.3:n.*945_*946del
NM_000168.5:c.*945_*946del	NP_000159.3:n.*945_*946del
XM_005249703.1:c.*945_*946del	XP_005249760.1:n.*945_*946del
XM_005249704.2:c.*945_*946del	XP_005249761.1:n.*945_*946del
XM_011515272.1:c.*945_*946del	XP_011513574.1:n.*945_*946del
XM_011515273.1:c.*945_*946del	XP_011513575.1:n.*945_*946del
XM_011515274.1:c.*945_*946del	XP_011513576.1:n.*945_*946del
NM_000168.6:c.*945_*946del MANE Select	NP_000159.3:n.*945_*946del