Canonical Allele Identifier: CA4230283

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41965339T>C , CM000669.2:g.41965339T>C	GRCh38
NC_000007.13:g.42004937T>C , CM000669.1:g.42004937T>C	GRCh37
NC_000007.12:g.41971462T>C	NCBI36
NG_008434.1:g.276682A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000168.6:c.3734A>G MANE Select	NP_000159.3:p.His1245Arg
ENST00000395925.8:c.3734A>G MANE Select	ENSP00000379258.3:p.His1245Arg
NM_000168.5:c.3734A>G	NP_000159.3:p.His1245Arg
ENST00000395925.7:c.3734A>G	ENSP00000379258.3:p.His1245Arg
ENST00000479210.1:n.3711A>G
ENST00000677288.1:c.3560A>G	ENSP00000503986.1:p.His1187Arg
ENST00000677605.1:c.3734A>G	ENSP00000503743.1:p.His1245Arg
ENST00000678429.1:c.3734A>G	ENSP00000502957.1:p.His1245Arg
XM_005249703.1:c.3734A>G	XP_005249760.1:p.His1245Arg
XM_005249704.2:c.3734A>G	XP_005249761.1:p.His1245Arg
XM_011515272.1:c.3734A>G	XP_011513574.1:p.His1245Arg
XM_011515273.1:c.3734A>G	XP_011513575.1:p.His1245Arg
XM_011515274.1:c.3557A>G	XP_011513576.1:p.His1186Arg
XM_011515274.2:c.3557A>G	XP_011513576.1:p.His1186Arg
XM_017011997.1:c.3731A>G	XP_016867486.1:p.His1244Arg