Canonical Allele Identifier: CA1702660145

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41964199_41964201delinsAAC , CM000669.2:g.41964199_41964201delinsAAC	GRCh38
NC_000007.13:g.42003797_42003799delinsAAC , CM000669.1:g.42003797_42003799delinsAAC	GRCh37
NC_000007.12:g.41970322_41970324delinsAAC	NCBI36
NG_008434.1:g.277820_277822delinsGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.*129_*131delinsGTT MANE Select	ENSP00000379258.3:n.*129_*131delinsGTT
ENST00000677288.1:c.*129_*131delinsGTT	ENSP00000503986.1:n.*129_*131delinsGTT
ENST00000677605.1:c.*129_*131delinsGTT	ENSP00000503743.1:n.*129_*131delinsGTT
ENST00000678429.1:c.*129_*131delinsGTT	ENSP00000502957.1:n.*129_*131delinsGTT
ENST00000395925.7:c.*129_*131delinsGTT	ENSP00000379258.3:n.*129_*131delinsGTT
ENST00000479210.1:n.4849_4851delinsGTT
NM_000168.5:c.*129_*131delinsGTT	NP_000159.3:n.*129_*131delinsGTT
XM_005249703.1:c.*129_*131delinsGTT	XP_005249760.1:n.*129_*131delinsGTT
XM_005249704.2:c.*129_*131delinsGTT	XP_005249761.1:n.*129_*131delinsGTT
XM_011515272.1:c.*129_*131delinsGTT	XP_011513574.1:n.*129_*131delinsGTT
XM_011515273.1:c.*129_*131delinsGTT	XP_011513575.1:n.*129_*131delinsGTT
XM_011515274.1:c.*129_*131delinsGTT	XP_011513576.1:n.*129_*131delinsGTT
NM_000168.6:c.*129_*131delinsGTT MANE Select	NP_000159.3:n.*129_*131delinsGTT