Canonical Allele Identifier: CA1702647690

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972381_41972382delinsCC , CM000669.2:g.41972381_41972382delinsCC	GRCh38
NC_000007.13:g.42011980_42011981delinsCC , CM000669.1:g.42011980_42011981delinsCC	GRCh37
NC_000007.12:g.41978505_41978506delinsCC	NCBI36
NG_008434.1:g.269638_269639delinsGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.2058_2059delinsGG MANE Select	ENSP00000379258.3:p.Arg686=
ENST00000677288.1:c.1884_1885delinsGG	ENSP00000503986.1:p.Arg628=
ENST00000677605.1:c.2058_2059delinsGG	ENSP00000503743.1:p.Arg686=
ENST00000678429.1:c.2058_2059delinsGG	ENSP00000502957.1:p.Arg686=
ENST00000395925.7:c.2058_2059delinsGG	ENSP00000379258.3:p.Arg686=
ENST00000479210.1:n.2035_2036delinsGG
NM_000168.5:c.2058_2059delinsGG	NP_000159.3:p.Arg686=
XM_005249703.1:c.2058_2059delinsGG	XP_005249760.1:p.Arg686=
XM_005249704.2:c.2058_2059delinsGG	XP_005249761.1:p.Arg686=
XM_011515272.1:c.2058_2059delinsGG	XP_011513574.1:p.Arg686=
XM_011515273.1:c.2058_2059delinsGG	XP_011513575.1:p.Arg686=
XM_011515274.1:c.1881_1882delinsGG	XP_011513576.1:p.Arg627=
XM_011515274.2:c.1881_1882delinsGG	XP_011513576.1:p.Arg627=
XM_017011997.1:c.2055_2056delinsGG	XP_016867486.1:p.Arg685=
NM_000168.6:c.2058_2059delinsGG MANE Select	NP_000159.3:p.Arg686=