Canonical Allele Identifier: CA1702660973

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41965863G= , CM000669.2:g.41965863G=	GRCh38
NC_000007.13:g.42005461G= , CM000669.1:g.42005461G=	GRCh37
NC_000007.12:g.41971986G=	NCBI36
NG_008434.1:g.276158C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.3210C= MANE Select	ENSP00000379258.3:p.Thr1070=
ENST00000677288.1:c.3036C=	ENSP00000503986.1:p.Thr1012=
ENST00000677605.1:c.3210C=	ENSP00000503743.1:p.Thr1070=
ENST00000678429.1:c.3210C=	ENSP00000502957.1:p.Thr1070=
ENST00000395925.7:c.3210C=	ENSP00000379258.3:p.Thr1070=
ENST00000479210.1:n.3187C=
NM_000168.5:c.3210C=	NP_000159.3:p.Thr1070=
XM_005249703.1:c.3210C=	XP_005249760.1:p.Thr1070=
XM_005249704.2:c.3210C=	XP_005249761.1:p.Thr1070=
XM_011515272.1:c.3210C=	XP_011513574.1:p.Thr1070=
XM_011515273.1:c.3210C=	XP_011513575.1:p.Thr1070=
XM_011515274.1:c.3033C=	XP_011513576.1:p.Thr1011=
XM_011515274.2:c.3033C=	XP_011513576.1:p.Thr1011=
XM_017011997.1:c.3207C=	XP_016867486.1:p.Thr1069=
NM_000168.6:c.3210C= MANE Select	NP_000159.3:p.Thr1070=