Canonical Allele Identifier: CA1702731850

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42148250T= , CM000669.2:g.42148250T=	GRCh38
NC_000007.13:g.42187849T= , CM000669.1:g.42187849T=	GRCh37
NC_000007.12:g.42154374T=	NCBI36
NG_008434.1:g.93770A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.343A= MANE Select	ENSP00000379258.3:p.Asn115=
ENST00000642432.1:c.166A=	ENSP00000495498.1:p.Asn56=
ENST00000643264.1:c.166A=	ENSP00000495207.1:p.Asn56=
ENST00000647255.1:c.166A=	ENSP00000495745.1:p.Asn56=
ENST00000677288.1:c.166A=	ENSP00000503986.1:p.Asn56=
ENST00000677605.1:c.343A=	ENSP00000503743.1:p.Asn115=
ENST00000678429.1:c.343A=	ENSP00000502957.1:p.Asn115=
ENST00000395925.7:c.343A=	ENSP00000379258.3:p.Asn115=
ENST00000448703.5:c.343A=	ENSP00000406135.1:p.Asn115=
ENST00000479210.1:n.320A=
NM_000168.5:c.343A=	NP_000159.3:p.Asn115=
XM_005249703.1:c.343A=	XP_005249760.1:p.Asn115=
XM_005249704.2:c.343A=	XP_005249761.1:p.Asn115=
XM_011515272.1:c.343A=	XP_011513574.1:p.Asn115=
XM_011515273.1:c.343A=	XP_011513575.1:p.Asn115=
XM_011515274.1:c.166A=	XP_011513576.1:p.Asn56=
XM_011515274.2:c.166A=	XP_011513576.1:p.Asn56=
XM_017011997.1:c.340A=	XP_016867486.1:p.Asn114=
NM_000168.6:c.343A= MANE Select	NP_000159.3:p.Asn115=