Canonical Allele Identifier: CA2682510199

Gene: GLI3

Linked Data

• gnomAD v4: 7-41972684-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972687dup , CM000669.2:g.41972687dup	GRCh38
NC_000007.13:g.42012286dup , CM000669.1:g.42012286dup	GRCh37
NC_000007.12:g.41978811dup	NCBI36
NG_008434.1:g.269335dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1813-58dup MANE Select	ENSP00000379258.3:n.1813-58dup
ENST00000677288.1:c.1639-58dup	ENSP00000503986.1:n.1639-58dup
ENST00000677605.1:c.1813-58dup	ENSP00000503743.1:n.1813-58dup
ENST00000678429.1:c.1813-58dup	ENSP00000502957.1:n.1813-58dup
ENST00000395925.7:c.1813-58dup	ENSP00000379258.3:n.1813-58dup
ENST00000464291.1:n.366-58dup
ENST00000479210.1:n.1790-58dup
NM_000168.5:c.1813-58dup	NP_000159.3:n.1813-58dup
XM_005249703.1:c.1813-58dup	XP_005249760.1:n.1813-58dup
XM_005249704.2:c.1813-58dup	XP_005249761.1:n.1813-58dup
XM_011515272.1:c.1813-58dup	XP_011513574.1:n.1813-58dup
XM_011515273.1:c.1813-58dup	XP_011513575.1:n.1813-58dup
XM_011515274.1:c.1636-58dup	XP_011513576.1:n.1636-58dup
XM_011515274.2:c.1636-58dup	XP_011513576.1:n.1636-58dup
XM_017011997.1:c.1810-58dup	XP_016867486.1:n.1810-58dup
NM_000168.6:c.1813-58dup MANE Select	NP_000159.3:n.1813-58dup