Canonical Allele Identifier: CA2775180374

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42048818_42048819insCCCAAACCAAACACACCCAACAC , CM000669.2:g.42048818_42048819insCCCAAACCAAACACACCCAACAC	GRCh38
NC_000007.13:g.42088417_42088418insCCCAAACCAAACACACCCAACAC , CM000669.1:g.42088417_42088418insCCCAAACCAAACACACCCAACAC	GRCh37
NC_000007.12:g.42054942_42054943insCCCAAACCAAACACACCCAACAC	NCBI36
NG_008434.1:g.193201_193202insGTGTTGGGTGTGTTTGGTTTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG MANE Select	ENSP00000379258.3:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG...
ENST00000677288.1:c.297-123_297-122insGTGTTGGGTGTGTTTGGTTTGGG	ENSP00000503986.1:n.297-123_297-122insGTGTTGGGTGTGTTTGGTTTGGG...
ENST00000677605.1:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG	ENSP00000503743.1:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG...
ENST00000678429.1:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG	ENSP00000502957.1:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG...
ENST00000395925.7:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG	ENSP00000379258.3:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG...
ENST00000448703.5:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG	ENSP00000406135.1:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG...
ENST00000479210.1:n.451-123_451-122insGTGTTGGGTGTGTTTGGTTTGGG
NM_000168.5:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG	NP_000159.3:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG
XM_005249703.1:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG	XP_005249760.1:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG
XM_005249704.2:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG	XP_005249761.1:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG
XM_011515272.1:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG	XP_011513574.1:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG
XM_011515273.1:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG	XP_011513575.1:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG
XM_011515274.1:c.297-123_297-122insGTGTTGGGTGTGTTTGGTTTGGG	XP_011513576.1:n.297-123_297-122insGTGTTGGGTGTGTTTGGTTTGGG
XM_011515274.2:c.297-123_297-122insGTGTTGGGTGTGTTTGGTTTGGG	XP_011513576.1:n.297-123_297-122insGTGTTGGGTGTGTTTGGTTTGGG
XM_017011997.1:c.471-123_471-122insGTGTTGGGTGTGTTTGGTTTGGG	XP_016867486.1:n.471-123_471-122insGTGTTGGGTGTGTTTGGTTTGGG
NM_000168.6:c.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG MANE Select	NP_000159.3:n.474-123_474-122insGTGTTGGGTGTGTTTGGTTTGGG