Canonical Allele Identifier: CA1100624209

Gene: GLI3

Linked Data

• dbSNP Id: rs1784099299
• gnomAD v3: 7-42040016-A-T
• gnomAD v4: 7-42040016-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42040016A>T , CM000669.2:g.42040016A>T	GRCh38
NC_000007.13:g.42079615A>T , CM000669.1:g.42079615A>T	GRCh37
NC_000007.12:g.42046140A>T	NCBI36
NG_008434.1:g.202004T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1028+22T>A MANE Select	ENSP00000379258.3:n.1028+22T>A
ENST00000677288.1:c.851+22T>A	ENSP00000503986.1:n.851+22T>A
ENST00000677605.1:c.1028+22T>A	ENSP00000503743.1:n.1028+22T>A
ENST00000678429.1:c.1028+22T>A	ENSP00000502957.1:n.1028+22T>A
ENST00000395925.7:c.1028+22T>A	ENSP00000379258.3:n.1028+22T>A
ENST00000479210.1:n.1005+22T>A
NM_000168.5:c.1028+22T>A	NP_000159.3:n.1028+22T>A
XM_005249703.1:c.1028+22T>A	XP_005249760.1:n.1028+22T>A
XM_005249704.2:c.1028+22T>A	XP_005249761.1:n.1028+22T>A
XM_011515272.1:c.1028+22T>A	XP_011513574.1:n.1028+22T>A
XM_011515273.1:c.1028+22T>A	XP_011513575.1:n.1028+22T>A
XM_011515274.1:c.851+22T>A	XP_011513576.1:n.851+22T>A
XM_011515274.2:c.851+22T>A	XP_011513576.1:n.851+22T>A
XM_017011997.1:c.1025+22T>A	XP_016867486.1:n.1025+22T>A
NM_000168.6:c.1028+22T>A MANE Select	NP_000159.3:n.1028+22T>A