Canonical Allele Identifier: CA1702775570

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42236998C= , CM000669.2:g.42236998C=	GRCh38
NC_000007.13:g.42276597C= , CM000669.1:g.42276597C=	GRCh37
NC_000007.12:g.42243122C=	NCBI36
NG_008434.1:g.5022G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.-70G= MANE Select	ENSP00000379258.3:n.-70G=
ENST00000428534.2:c.-43+786G=	ENSP00000503957.1:n.-43+786G=
ENST00000677605.1:c.-43+501G=	ENSP00000503743.1:n.-43+501G=
ENST00000677990.1:n.212G=
ENST00000678978.1:c.-42-13703G=	ENSP00000503352.1:n.-42-13703G=
ENST00000395925.7:c.-70G=	ENSP00000379258.3:n.-70G=
ENST00000428534.1:n.87+786G=
ENST00000437480.1:c.-70G=	ENSP00000407963.1:n.-70G=
NM_000168.5:c.-70G=	NP_000159.3:n.-70G=
XM_005249703.1:c.-43+786G=	XP_005249760.1:n.-43+786G=
XM_005249704.2:c.-43+501G=	XP_005249761.1:n.-43+501G=
XM_011515273.1:c.-42-13703G=	XP_011513575.1:n.-42-13703G=
NM_000168.6:c.-70G= MANE Select	NP_000159.3:n.-70G=