Canonical Allele Identifier: CA917990639

Gene: GLI3

Linked Data

• dbSNP Id: rs869118880

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41965989del , CM000669.2:g.41965989del	GRCh38
NC_000007.13:g.42005587del , CM000669.1:g.42005587del	GRCh37
NC_000007.12:g.41972112del	NCBI36
NG_008434.1:g.276032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.3084del MANE Select	ENSP00000379258.3:p.Ser1028ArgfsTer?
ENST00000677288.1:c.2910del	ENSP00000503986.1:p.Ser970ArgfsTer?
ENST00000677605.1:c.3084del	ENSP00000503743.1:p.Ser1028ArgfsTer?
ENST00000678429.1:c.3084del	ENSP00000502957.1:p.Ser1028ArgfsTer?
ENST00000395925.7:c.3084del	ENSP00000379258.3:p.Ser1028ArgfsTer?
ENST00000479210.1:n.3061del
NM_000168.5:c.3084del	NP_000159.3:p.Ser1028ArgfsTer?
XM_005249703.1:c.3084del	XP_005249760.1:p.Ser1028ArgfsTer?
XM_005249704.2:c.3084del	XP_005249761.1:p.Ser1028ArgfsTer?
XM_011515272.1:c.3084del	XP_011513574.1:p.Ser1028ArgfsTer?
XM_011515273.1:c.3084del	XP_011513575.1:p.Ser1028ArgfsTer?
XM_011515274.1:c.2907del	XP_011513576.1:p.Ser969ArgfsTer?
XM_011515274.2:c.2907del	XP_011513576.1:p.Ser969ArgfsTer?
XM_017011997.1:c.3081del	XP_016867486.1:p.Ser1027ArgfsTer?
NM_000168.6:c.3084del MANE Select	NP_000159.3:p.Ser1028ArgfsTer?