Canonical Allele Identifier: CA1702754145

Gene: GLI3

Linked Data

• dbSNP Id: rs1787801307

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42190279del , CM000669.2:g.42190279del	GRCh38
NC_000007.13:g.42229878del , CM000669.1:g.42229878del	GRCh37
NC_000007.12:g.42196403del	NCBI36
NG_008434.1:g.51742del

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.124+32852del MANE Select	ENSP00000379258.3:n.124+32852del
ENST00000677605.1:c.124+32852del	ENSP00000503743.1:n.124+32852del
ENST00000678429.1:c.124+32852del	ENSP00000502957.1:n.124+32852del
ENST00000395925.7:c.124+32852del	ENSP00000379258.3:n.124+32852del
ENST00000437480.1:c.125-17592del	ENSP00000407963.1:n.125-17592del
ENST00000448703.5:c.124+32852del	ENSP00000406135.1:n.124+32852del
NM_000168.5:c.124+32852del	NP_000159.3:n.124+32852del
XM_005249703.1:c.124+32852del	XP_005249760.1:n.124+32852del
XM_005249704.2:c.124+32852del	XP_005249761.1:n.124+32852del
XM_011515272.1:c.124+32852del	XP_011513574.1:n.124+32852del
XM_011515273.1:c.124+32852del	XP_011513575.1:n.124+32852del
NM_000168.6:c.124+32852del MANE Select	NP_000159.3:n.124+32852del