Canonical Allele Identifier: CA2695207661

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41966298_41966300del , CM000669.2:g.41966298_41966300del	GRCh38
NC_000007.13:g.42005896_42005898del , CM000669.1:g.42005896_42005898del	GRCh37
NC_000007.12:g.41972421_41972423del	NCBI36
NG_008434.1:g.275724_275726del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.2776_2778del MANE Select	ENSP00000379258.3:p.Gln926del
ENST00000677288.1:c.2602_2604del	ENSP00000503986.1:p.Gln868del
ENST00000677605.1:c.2776_2778del	ENSP00000503743.1:p.Gln926del
ENST00000678429.1:c.2776_2778del	ENSP00000502957.1:p.Gln926del
ENST00000395925.7:c.2776_2778del	ENSP00000379258.3:p.Gln926del
ENST00000479210.1:n.2753_2755del
NM_000168.5:c.2776_2778del	NP_000159.3:p.Gln926del
XM_005249703.1:c.2776_2778del	XP_005249760.1:p.Gln926del
XM_005249704.2:c.2776_2778del	XP_005249761.1:p.Gln926del
XM_011515272.1:c.2776_2778del	XP_011513574.1:p.Gln926del
XM_011515273.1:c.2776_2778del	XP_011513575.1:p.Gln926del
XM_011515274.1:c.2599_2601del	XP_011513576.1:p.Gln867del
XM_011515274.2:c.2599_2601del	XP_011513576.1:p.Gln867del
XM_017011997.1:c.2773_2775del	XP_016867486.1:p.Gln925del
NM_000168.6:c.2776_2778del MANE Select	NP_000159.3:p.Gln926del