Canonical Allele Identifier: CA1283796167

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990541C= , CM000664.2:g.120990541C=	GRCh38
NC_000002.11:g.121748117C= , CM000664.1:g.121748117C=	GRCh37
NC_000002.10:g.121464587C=	NCBI36
NG_009030.1:g.198251C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4576C= MANE Select	ENSP00000354586.5:p.Arg1526=
ENST00000452319.6:c.4627C=	ENSP00000390436.1:p.Arg1543=
ENST00000341310.10:c.*3675C=	ENSP00000344473.6:n.*3675C=
ENST00000361492.8:c.4627C=	ENSP00000354586.4:p.Arg1543=
ENST00000438299.5:c.*2544-49C=	ENSP00000400593.1:n.*2544-49C=
ENST00000445186.5:c.*3726C=	ENSP00000397488.1:n.*3726C=
ENST00000452319.5:c.4627C=	ENSP00000390436.1:p.Arg1543=
ENST00000452692.5:c.*2493-49C=	ENSP00000403715.1:n.*2493-49C=
NM_005270.4:c.4627C=	NP_005261.2:p.Arg1543=
XM_006712422.1:c.4576C=	XP_006712485.1:p.Arg1526=
XM_011510969.1:c.4609C=	XP_011509271.1:p.Arg1537=
XM_011510970.1:c.4486C=	XP_011509272.1:p.Arg1496=
XM_011510971.1:c.4432C=	XP_011509273.1:p.Arg1478=
XM_011510972.1:c.4432C=	XP_011509274.1:p.Arg1478=
XM_011510973.1:c.4252C=	XP_011509275.1:p.Arg1418=
XM_011510974.1:c.4201C=	XP_011509276.1:p.Arg1401=
XM_006712422.3:c.4576C=	XP_006712485.1:p.Arg1526=
XM_011510969.2:c.4879C=	XP_011509271.2:p.Arg1627=
XM_011510970.2:c.4486C=	XP_011509272.1:p.Arg1496=
XM_011510971.2:c.4432C=	XP_011509273.1:p.Arg1478=
XM_011510972.2:c.4528C=	XP_011509274.2:p.Arg1510=
XM_011510973.2:c.4252C=	XP_011509275.1:p.Arg1418=
XM_011510974.2:c.4201C=	XP_011509276.1:p.Arg1401=
XM_017003818.1:c.4828C=	XP_016859307.1:p.Arg1610=
XM_024452794.1:c.4627C=	XP_024308562.1:p.Arg1543=
XM_024452795.1:c.4627C=	XP_024308563.1:p.Arg1543=
NM_001371271.1:c.4627C=	NP_001358200.1:p.Arg1543=
NM_001374353.1:c.4576C= MANE Select	NP_001361282.1:p.Arg1526=
NM_001374354.1:c.4201C=	NP_001361283.1:p.Arg1401=
NM_005270.5:c.4627C=	NP_005261.2:p.Arg1543=