Canonical Allele Identifier: CA1702691326

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42040184_42040189delinsCAGTGT , CM000669.2:g.42040184_42040189delinsCAGTGT	GRCh38
NC_000007.13:g.42079783_42079788delinsCAGTGT , CM000669.1:g.42079783_42079788delinsCAGTGT	GRCh37
NC_000007.12:g.42046308_42046313delinsCAGTGT	NCBI36
NG_008434.1:g.201831_201836delinsACACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.877_882delinsACACTG MANE Select	ENSP00000379258.3:p.Thr293=
ENST00000677288.1:c.700_705delinsACACTG	ENSP00000503986.1:p.Thr234=
ENST00000677605.1:c.877_882delinsACACTG	ENSP00000503743.1:p.Thr293=
ENST00000678429.1:c.877_882delinsACACTG	ENSP00000502957.1:p.Thr293=
ENST00000395925.7:c.877_882delinsACACTG	ENSP00000379258.3:p.Thr293=
ENST00000479210.1:n.854_859delinsACACTG
NM_000168.5:c.877_882delinsACACTG	NP_000159.3:p.Thr293=
XM_005249703.1:c.877_882delinsACACTG	XP_005249760.1:p.Thr293=
XM_005249704.2:c.877_882delinsACACTG	XP_005249761.1:p.Thr293=
XM_011515272.1:c.877_882delinsACACTG	XP_011513574.1:p.Thr293=
XM_011515273.1:c.877_882delinsACACTG	XP_011513575.1:p.Thr293=
XM_011515274.1:c.700_705delinsACACTG	XP_011513576.1:p.Thr234=
XM_011515274.2:c.700_705delinsACACTG	XP_011513576.1:p.Thr234=
XM_017011997.1:c.874_879delinsACACTG	XP_016867486.1:p.Thr292=
NM_000168.6:c.877_882delinsACACTG MANE Select	NP_000159.3:p.Thr293=