Canonical Allele Identifier: CA1283796139

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990480G= , CM000664.2:g.120990480G=	GRCh38
NC_000002.11:g.121748056G= , CM000664.1:g.121748056G=	GRCh37
NC_000002.10:g.121464526G=	NCBI36
NG_009030.1:g.198190G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4515G= MANE Select	ENSP00000354586.5:p.Ser1505=
ENST00000452319.6:c.4566G=	ENSP00000390436.1:p.Ser1522=
ENST00000341310.10:c.*3614G=	ENSP00000344473.6:n.*3614G=
ENST00000361492.8:c.4566G=	ENSP00000354586.4:p.Ser1522=
ENST00000438299.5:c.*2544-110G=	ENSP00000400593.1:n.*2544-110G=
ENST00000445186.5:c.*3665G=	ENSP00000397488.1:n.*3665G=
ENST00000452319.5:c.4566G=	ENSP00000390436.1:p.Ser1522=
ENST00000452692.5:c.*2493-110G=	ENSP00000403715.1:n.*2493-110G=
NM_005270.4:c.4566G=	NP_005261.2:p.Ser1522=
XM_006712422.1:c.4515G=	XP_006712485.1:p.Ser1505=
XM_011510969.1:c.4548G=	XP_011509271.1:p.Ser1516=
XM_011510970.1:c.4425G=	XP_011509272.1:p.Ser1475=
XM_011510971.1:c.4371G=	XP_011509273.1:p.Ser1457=
XM_011510972.1:c.4371G=	XP_011509274.1:p.Ser1457=
XM_011510973.1:c.4191G=	XP_011509275.1:p.Ser1397=
XM_011510974.1:c.4140G=	XP_011509276.1:p.Ser1380=
XM_006712422.3:c.4515G=	XP_006712485.1:p.Ser1505=
XM_011510969.2:c.4818G=	XP_011509271.2:p.Ser1606=
XM_011510970.2:c.4425G=	XP_011509272.1:p.Ser1475=
XM_011510971.2:c.4371G=	XP_011509273.1:p.Ser1457=
XM_011510972.2:c.4467G=	XP_011509274.2:p.Ser1489=
XM_011510973.2:c.4191G=	XP_011509275.1:p.Ser1397=
XM_011510974.2:c.4140G=	XP_011509276.1:p.Ser1380=
XM_017003818.1:c.4767G=	XP_016859307.1:p.Ser1589=
XM_024452794.1:c.4566G=	XP_024308562.1:p.Ser1522=
XM_024452795.1:c.4566G=	XP_024308563.1:p.Ser1522=
NM_001371271.1:c.4566G=	NP_001358200.1:p.Ser1522=
NM_001374353.1:c.4515G= MANE Select	NP_001361282.1:p.Ser1505=
NM_001374354.1:c.4140G=	NP_001361283.1:p.Ser1380=
NM_005270.5:c.4566G=	NP_005261.2:p.Ser1522=