Canonical Allele Identifier: CA1283796209

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990632C= , CM000664.2:g.120990632C=	GRCh38
NC_000002.11:g.121748208C= , CM000664.1:g.121748208C=	GRCh37
NC_000002.10:g.121464678C=	NCBI36
NG_009030.1:g.198342C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4667C= MANE Select	ENSP00000354586.5:p.Thr1556=
ENST00000452319.6:c.4718C=	ENSP00000390436.1:p.Thr1573=
ENST00000341310.10:c.*3766C=	ENSP00000344473.6:n.*3766C=
ENST00000361492.8:c.4718C=	ENSP00000354586.4:p.Thr1573=
ENST00000438299.5:c.*2586C=	ENSP00000400593.1:n.*2586C=
ENST00000445186.5:c.*3817C=	ENSP00000397488.1:n.*3817C=
ENST00000452319.5:c.4718C=	ENSP00000390436.1:p.Thr1573=
ENST00000452692.5:c.*2535C=	ENSP00000403715.1:n.*2535C=
NM_005270.4:c.4718C=	NP_005261.2:p.Thr1573=
XM_006712422.1:c.4667C=	XP_006712485.1:p.Thr1556=
XM_011510969.1:c.4700C=	XP_011509271.1:p.Thr1567=
XM_011510970.1:c.4577C=	XP_011509272.1:p.Thr1526=
XM_011510971.1:c.4523C=	XP_011509273.1:p.Thr1508=
XM_011510972.1:c.4523C=	XP_011509274.1:p.Thr1508=
XM_011510973.1:c.4343C=	XP_011509275.1:p.Thr1448=
XM_011510974.1:c.4292C=	XP_011509276.1:p.Thr1431=
XM_006712422.3:c.4667C=	XP_006712485.1:p.Thr1556=
XM_011510969.2:c.4970C=	XP_011509271.2:p.Thr1657=
XM_011510970.2:c.4577C=	XP_011509272.1:p.Thr1526=
XM_011510971.2:c.4523C=	XP_011509273.1:p.Thr1508=
XM_011510972.2:c.4619C=	XP_011509274.2:p.Thr1540=
XM_011510973.2:c.4343C=	XP_011509275.1:p.Thr1448=
XM_011510974.2:c.4292C=	XP_011509276.1:p.Thr1431=
XM_017003818.1:c.4919C=	XP_016859307.1:p.Thr1640=
XM_024452794.1:c.4718C=	XP_024308562.1:p.Thr1573=
XM_024452795.1:c.4718C=	XP_024308563.1:p.Thr1573=
NM_001371271.1:c.4718C=	NP_001358200.1:p.Thr1573=
NM_001374353.1:c.4667C= MANE Select	NP_001361282.1:p.Thr1556=
NM_001374354.1:c.4292C=	NP_001361283.1:p.Thr1431=
NM_005270.5:c.4718C=	NP_005261.2:p.Thr1573=