Canonical Allele Identifier: CA1702647830

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972442G= , CM000669.2:g.41972442G=	GRCh38
NC_000007.13:g.42012041G= , CM000669.1:g.42012041G=	GRCh37
NC_000007.12:g.41978566G=	NCBI36
NG_008434.1:g.269578C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1998C= MANE Select	ENSP00000379258.3:p.Gly666=
ENST00000677288.1:c.1824C=	ENSP00000503986.1:p.Gly608=
ENST00000677605.1:c.1998C=	ENSP00000503743.1:p.Gly666=
ENST00000678429.1:c.1998C=	ENSP00000502957.1:p.Gly666=
ENST00000395925.7:c.1998C=	ENSP00000379258.3:p.Gly666=
ENST00000464291.1:n.551C=
ENST00000479210.1:n.1975C=
NM_000168.5:c.1998C=	NP_000159.3:p.Gly666=
XM_005249703.1:c.1998C=	XP_005249760.1:p.Gly666=
XM_005249704.2:c.1998C=	XP_005249761.1:p.Gly666=
XM_011515272.1:c.1998C=	XP_011513574.1:p.Gly666=
XM_011515273.1:c.1998C=	XP_011513575.1:p.Gly666=
XM_011515274.1:c.1821C=	XP_011513576.1:p.Gly607=
XM_011515274.2:c.1821C=	XP_011513576.1:p.Gly607=
XM_017011997.1:c.1995C=	XP_016867486.1:p.Gly665=
NM_000168.6:c.1998C= MANE Select	NP_000159.3:p.Gly666=