Canonical Allele Identifier: CA1702647835

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972445A= , CM000669.2:g.41972445A=	GRCh38
NC_000007.13:g.42012044A= , CM000669.1:g.42012044A=	GRCh37
NC_000007.12:g.41978569A=	NCBI36
NG_008434.1:g.269575T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1995T= MANE Select	ENSP00000379258.3:p.Pro665=
ENST00000677288.1:c.1821T=	ENSP00000503986.1:p.Pro607=
ENST00000677605.1:c.1995T=	ENSP00000503743.1:p.Pro665=
ENST00000678429.1:c.1995T=	ENSP00000502957.1:p.Pro665=
ENST00000395925.7:c.1995T=	ENSP00000379258.3:p.Pro665=
ENST00000464291.1:n.548T=
ENST00000479210.1:n.1972T=
NM_000168.5:c.1995T=	NP_000159.3:p.Pro665=
XM_005249703.1:c.1995T=	XP_005249760.1:p.Pro665=
XM_005249704.2:c.1995T=	XP_005249761.1:p.Pro665=
XM_011515272.1:c.1995T=	XP_011513574.1:p.Pro665=
XM_011515273.1:c.1995T=	XP_011513575.1:p.Pro665=
XM_011515274.1:c.1818T=	XP_011513576.1:p.Pro606=
XM_011515274.2:c.1818T=	XP_011513576.1:p.Pro606=
XM_017011997.1:c.1992T=	XP_016867486.1:p.Pro664=
NM_000168.6:c.1995T= MANE Select	NP_000159.3:p.Pro665=