Canonical Allele Identifier: CA1702691876

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42040567_42040570delinsCATT , CM000669.2:g.42040567_42040570delinsCATT	GRCh38
NC_000007.13:g.42080166_42080169delinsCATT , CM000669.1:g.42080166_42080169delinsCATT	GRCh37
NC_000007.12:g.42046691_42046694delinsCATT	NCBI36
NG_008434.1:g.201450_201453delinsAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.827-331_827-328delinsAATG MANE Select	ENSP00000379258.3:n.827-331_827-328delinsAATG
ENST00000677288.1:c.650-331_650-328delinsAATG	ENSP00000503986.1:n.650-331_650-328delinsAATG
ENST00000677605.1:c.827-331_827-328delinsAATG	ENSP00000503743.1:n.827-331_827-328delinsAATG
ENST00000678429.1:c.827-331_827-328delinsAATG	ENSP00000502957.1:n.827-331_827-328delinsAATG
ENST00000395925.7:c.827-331_827-328delinsAATG	ENSP00000379258.3:n.827-331_827-328delinsAATG
ENST00000479210.1:n.804-331_804-328delinsAATG
NM_000168.5:c.827-331_827-328delinsAATG	NP_000159.3:n.827-331_827-328delinsAATG
XM_005249703.1:c.827-331_827-328delinsAATG	XP_005249760.1:n.827-331_827-328delinsAATG
XM_005249704.2:c.827-331_827-328delinsAATG	XP_005249761.1:n.827-331_827-328delinsAATG
XM_011515272.1:c.827-331_827-328delinsAATG	XP_011513574.1:n.827-331_827-328delinsAATG
XM_011515273.1:c.827-331_827-328delinsAATG	XP_011513575.1:n.827-331_827-328delinsAATG
XM_011515274.1:c.650-331_650-328delinsAATG	XP_011513576.1:n.650-331_650-328delinsAATG
XM_011515274.2:c.650-331_650-328delinsAATG	XP_011513576.1:n.650-331_650-328delinsAATG
XM_017011997.1:c.824-331_824-328delinsAATG	XP_016867486.1:n.824-331_824-328delinsAATG
NM_000168.6:c.827-331_827-328delinsAATG MANE Select	NP_000159.3:n.827-331_827-328delinsAATG