Canonical Allele Identifier: CA1702660371

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41964637A= , CM000669.2:g.41964637A=	GRCh38
NC_000007.13:g.42004235A= , CM000669.1:g.42004235A=	GRCh37
NC_000007.12:g.41970760A=	NCBI36
NG_008434.1:g.277384T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.4436T= MANE Select	ENSP00000379258.3:p.Leu1479=
ENST00000677288.1:c.4262T=	ENSP00000503986.1:p.Leu1421=
ENST00000677605.1:c.4436T=	ENSP00000503743.1:p.Leu1479=
ENST00000678429.1:c.4436T=	ENSP00000502957.1:p.Leu1479=
ENST00000395925.7:c.4436T=	ENSP00000379258.3:p.Leu1479=
ENST00000479210.1:n.4413T=
NM_000168.5:c.4436T=	NP_000159.3:p.Leu1479=
XM_005249703.1:c.4436T=	XP_005249760.1:p.Leu1479=
XM_005249704.2:c.4436T=	XP_005249761.1:p.Leu1479=
XM_011515272.1:c.4436T=	XP_011513574.1:p.Leu1479=
XM_011515273.1:c.4436T=	XP_011513575.1:p.Leu1479=
XM_011515274.1:c.4259T=	XP_011513576.1:p.Leu1420=
XM_011515274.2:c.4259T=	XP_011513576.1:p.Leu1420=
XM_017011997.1:c.4433T=	XP_016867486.1:p.Leu1478=
NM_000168.6:c.4436T= MANE Select	NP_000159.3:p.Leu1479=