Canonical Allele Identifier: CA1702647698

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972383C= , CM000669.2:g.41972383C=	GRCh38
NC_000007.13:g.42011982C= , CM000669.1:g.42011982C=	GRCh37
NC_000007.12:g.41978507C=	NCBI36
NG_008434.1:g.269637G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.2057G= MANE Select	ENSP00000379258.3:p.Arg686=
ENST00000677288.1:c.1883G=	ENSP00000503986.1:p.Arg628=
ENST00000677605.1:c.2057G=	ENSP00000503743.1:p.Arg686=
ENST00000678429.1:c.2057G=	ENSP00000502957.1:p.Arg686=
ENST00000395925.7:c.2057G=	ENSP00000379258.3:p.Arg686=
ENST00000479210.1:n.2034G=
NM_000168.5:c.2057G=	NP_000159.3:p.Arg686=
XM_005249703.1:c.2057G=	XP_005249760.1:p.Arg686=
XM_005249704.2:c.2057G=	XP_005249761.1:p.Arg686=
XM_011515272.1:c.2057G=	XP_011513574.1:p.Arg686=
XM_011515273.1:c.2057G=	XP_011513575.1:p.Arg686=
XM_011515274.1:c.1880G=	XP_011513576.1:p.Arg627=
XM_011515274.2:c.1880G=	XP_011513576.1:p.Arg627=
XM_017011997.1:c.2054G=	XP_016867486.1:p.Arg685=
NM_000168.6:c.2057G= MANE Select	NP_000159.3:p.Arg686=