Canonical Allele Identifier: CA1702661101

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41966079_41966080delinsCG , CM000669.2:g.41966079_41966080delinsCG	GRCh38
NC_000007.13:g.42005677_42005678delinsCG , CM000669.1:g.42005677_42005678delinsCG	GRCh37
NC_000007.12:g.41972202_41972203delinsCG	NCBI36
NG_008434.1:g.275941_275942delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.2993_2994delinsCG MANE Select	ENSP00000379258.3:p.Pro998=
ENST00000677288.1:c.2819_2820delinsCG	ENSP00000503986.1:p.Pro940=
ENST00000677605.1:c.2993_2994delinsCG	ENSP00000503743.1:p.Pro998=
ENST00000678429.1:c.2993_2994delinsCG	ENSP00000502957.1:p.Pro998=
ENST00000395925.7:c.2993_2994delinsCG	ENSP00000379258.3:p.Pro998=
ENST00000479210.1:n.2970_2971delinsCG
NM_000168.5:c.2993_2994delinsCG	NP_000159.3:p.Pro998=
XM_005249703.1:c.2993_2994delinsCG	XP_005249760.1:p.Pro998=
XM_005249704.2:c.2993_2994delinsCG	XP_005249761.1:p.Pro998=
XM_011515272.1:c.2993_2994delinsCG	XP_011513574.1:p.Pro998=
XM_011515273.1:c.2993_2994delinsCG	XP_011513575.1:p.Pro998=
XM_011515274.1:c.2816_2817delinsCG	XP_011513576.1:p.Pro939=
XM_011515274.2:c.2816_2817delinsCG	XP_011513576.1:p.Pro939=
XM_017011997.1:c.2990_2991delinsCG	XP_016867486.1:p.Pro997=
NM_000168.6:c.2993_2994delinsCG MANE Select	NP_000159.3:p.Pro998=