Canonical Allele Identifier: CA2580077123

Gene: GLI3

Linked Data

• ClinVar Variation Id: 2031540
• ClinVar RCV Id: RCV002898865

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42048622del , CM000669.2:g.42048622del	GRCh38
NC_000007.13:g.42088221del , CM000669.1:g.42088221del	GRCh37
NC_000007.12:g.42054746del	NCBI36
NG_008434.1:g.193398del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.548del MANE Select	ENSP00000379258.3:p.Thr183MetfsTer?
ENST00000677288.1:c.371del	ENSP00000503986.1:p.Thr124MetfsTer?
ENST00000677605.1:c.548del	ENSP00000503743.1:p.Thr183MetfsTer?
ENST00000678429.1:c.548del	ENSP00000502957.1:p.Thr183MetfsTer?
ENST00000395925.7:c.548del	ENSP00000379258.3:p.Thr183MetfsTer?
ENST00000479210.1:n.525del
NM_000168.5:c.548del	NP_000159.3:p.Thr183MetfsTer?
XM_005249703.1:c.548del	XP_005249760.1:p.Thr183MetfsTer?
XM_005249704.2:c.548del	XP_005249761.1:p.Thr183MetfsTer?
XM_011515272.1:c.548del	XP_011513574.1:p.Thr183MetfsTer?
XM_011515273.1:c.548del	XP_011513575.1:p.Thr183MetfsTer?
XM_011515274.1:c.371del	XP_011513576.1:p.Thr124MetfsTer?
XM_011515274.2:c.371del	XP_011513576.1:p.Thr124MetfsTer?
XM_017011997.1:c.545del	XP_016867486.1:p.Thr182MetfsTer?
NM_000168.6:c.548del MANE Select	NP_000159.3:p.Thr183MetfsTer?