Canonical Allele Identifier: CA1283790686

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120978544C= , CM000664.2:g.120978544C=	GRCh38
NC_000002.11:g.121736120C= , CM000664.1:g.121736120C=	GRCh37
NC_000002.10:g.121452590C=	NCBI36
NG_009030.1:g.186254C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.1428C= MANE Select	ENSP00000354586.5:p.His476=
ENST00000452319.6:c.1479C=	ENSP00000390436.1:p.His493=
ENST00000314490.15:c.492C=	ENSP00000312694.12:p.His164=
ENST00000341310.10:c.*527C=	ENSP00000344473.6:n.*527C=
ENST00000361492.8:c.1479C=	ENSP00000354586.4:p.His493=
ENST00000435313.6:n.1453C=
ENST00000437950.5:c.*578C=	ENSP00000415773.1:n.*578C=
ENST00000438299.5:c.*578C=	ENSP00000400593.1:n.*578C=
ENST00000445186.5:c.*578C=	ENSP00000397488.1:n.*578C=
ENST00000452319.5:c.1479C=	ENSP00000390436.1:p.His493=
ENST00000452692.5:c.*527C=	ENSP00000403715.1:n.*527C=
NM_005270.4:c.1479C=	NP_005261.2:p.His493=
XM_006712422.1:c.1428C=	XP_006712485.1:p.His476=
XM_011510969.1:c.1461C=	XP_011509271.1:p.His487=
XM_011510970.1:c.1338C=	XP_011509272.1:p.His446=
XM_011510971.1:c.1284C=	XP_011509273.1:p.His428=
XM_011510972.1:c.1284C=	XP_011509274.1:p.His428=
XM_011510973.1:c.1104C=	XP_011509275.1:p.His368=
XM_011510974.1:c.1053C=	XP_011509276.1:p.His351=
XM_006712422.3:c.1428C=	XP_006712485.1:p.His476=
XM_011510969.2:c.1731C=	XP_011509271.2:p.His577=
XM_011510970.2:c.1338C=	XP_011509272.1:p.His446=
XM_011510971.2:c.1284C=	XP_011509273.1:p.His428=
XM_011510972.2:c.1380C=	XP_011509274.2:p.His460=
XM_011510973.2:c.1104C=	XP_011509275.1:p.His368=
XM_011510974.2:c.1053C=	XP_011509276.1:p.His351=
XM_017003818.1:c.1680C=	XP_016859307.1:p.His560=
XM_024452794.1:c.1479C=	XP_024308562.1:p.His493=
XM_024452795.1:c.1479C=	XP_024308563.1:p.His493=
NM_001371271.1:c.1479C=	NP_001358200.1:p.His493=
NM_001374353.1:c.1428C= MANE Select	NP_001361282.1:p.His476=
NM_001374354.1:c.1053C=	NP_001361283.1:p.His351=
NM_005270.5:c.1479C=	NP_005261.2:p.His493=