Canonical Allele Identifier: CA838631207

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42223215_42223217del , CM000669.2:g.42223215_42223217del	GRCh38
NC_000007.13:g.42262814_42262816del , CM000669.1:g.42262814_42262816del	GRCh37
NC_000007.12:g.42229339_42229341del	NCBI36
NG_008434.1:g.18805_18807del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.39_41del MANE Select	ENSP00000379258.3:p.Lys14del
ENST00000428534.2:c.39_41del	ENSP00000503957.1:p.Lys14del
ENST00000677605.1:c.39_41del	ENSP00000503743.1:p.Lys14del
ENST00000678429.1:c.39_41del	ENSP00000502957.1:p.Lys14del
ENST00000678978.1:c.39_41del	ENSP00000503352.1:p.Lys14del
ENST00000395925.7:c.39_41del	ENSP00000379258.3:p.Lys14del
ENST00000428534.1:n.168_170del
ENST00000437480.1:c.39_41del	ENSP00000407963.1:p.Lys14del
ENST00000448703.5:c.39_41del	ENSP00000406135.1:p.Lys14del
NM_000168.5:c.39_41del	NP_000159.3:p.Lys14del
XM_005249703.1:c.39_41del	XP_005249760.1:p.Lys14del
XM_005249704.2:c.39_41del	XP_005249761.1:p.Lys14del
XM_011515272.1:c.39_41del	XP_011513574.1:p.Lys14del
XM_011515273.1:c.39_41del	XP_011513575.1:p.Lys14del
NM_000168.6:c.39_41del MANE Select	NP_000159.3:p.Lys14del