Canonical Allele Identifier: CA2578873965

Gene: GLI3

Linked Data

• gnomAD v4: 7-41972714-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972719del , CM000669.2:g.41972719del	GRCh38
NC_000007.13:g.42012318del , CM000669.1:g.42012318del	GRCh37
NC_000007.12:g.41978843del	NCBI36
NG_008434.1:g.269305del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1813-88del MANE Select	ENSP00000379258.3:n.1813-88del
ENST00000677288.1:c.1639-88del	ENSP00000503986.1:n.1639-88del
ENST00000677605.1:c.1813-88del	ENSP00000503743.1:n.1813-88del
ENST00000678429.1:c.1813-88del	ENSP00000502957.1:n.1813-88del
ENST00000395925.7:c.1813-88del	ENSP00000379258.3:n.1813-88del
ENST00000464291.1:n.366-88del
ENST00000479210.1:n.1790-88del
NM_000168.5:c.1813-88del	NP_000159.3:n.1813-88del
XM_005249703.1:c.1813-88del	XP_005249760.1:n.1813-88del
XM_005249704.2:c.1813-88del	XP_005249761.1:n.1813-88del
XM_011515272.1:c.1813-88del	XP_011513574.1:n.1813-88del
XM_011515273.1:c.1813-88del	XP_011513575.1:n.1813-88del
XM_011515274.1:c.1636-88del	XP_011513576.1:n.1636-88del
XM_011515274.2:c.1636-88del	XP_011513576.1:n.1636-88del
XM_017011997.1:c.1810-88del	XP_016867486.1:n.1810-88del
NM_000168.6:c.1813-88del MANE Select	NP_000159.3:n.1813-88del