Canonical Allele Identifier: CA1283796195

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990608T= , CM000664.2:g.120990608T=	GRCh38
NC_000002.11:g.121748184T= , CM000664.1:g.121748184T=	GRCh37
NC_000002.10:g.121464654T=	NCBI36
NG_009030.1:g.198318T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4643T= MANE Select	ENSP00000354586.5:p.Val1548=
ENST00000452319.6:c.4694T=	ENSP00000390436.1:p.Val1565=
ENST00000341310.10:c.*3742T=	ENSP00000344473.6:n.*3742T=
ENST00000361492.8:c.4694T=	ENSP00000354586.4:p.Val1565=
ENST00000438299.5:c.*2562T=	ENSP00000400593.1:n.*2562T=
ENST00000445186.5:c.*3793T=	ENSP00000397488.1:n.*3793T=
ENST00000452319.5:c.4694T=	ENSP00000390436.1:p.Val1565=
ENST00000452692.5:c.*2511T=	ENSP00000403715.1:n.*2511T=
NM_005270.4:c.4694T=	NP_005261.2:p.Val1565=
XM_006712422.1:c.4643T=	XP_006712485.1:p.Val1548=
XM_011510969.1:c.4676T=	XP_011509271.1:p.Val1559=
XM_011510970.1:c.4553T=	XP_011509272.1:p.Val1518=
XM_011510971.1:c.4499T=	XP_011509273.1:p.Val1500=
XM_011510972.1:c.4499T=	XP_011509274.1:p.Val1500=
XM_011510973.1:c.4319T=	XP_011509275.1:p.Val1440=
XM_011510974.1:c.4268T=	XP_011509276.1:p.Val1423=
XM_006712422.3:c.4643T=	XP_006712485.1:p.Val1548=
XM_011510969.2:c.4946T=	XP_011509271.2:p.Val1649=
XM_011510970.2:c.4553T=	XP_011509272.1:p.Val1518=
XM_011510971.2:c.4499T=	XP_011509273.1:p.Val1500=
XM_011510972.2:c.4595T=	XP_011509274.2:p.Val1532=
XM_011510973.2:c.4319T=	XP_011509275.1:p.Val1440=
XM_011510974.2:c.4268T=	XP_011509276.1:p.Val1423=
XM_017003818.1:c.4895T=	XP_016859307.1:p.Val1632=
XM_024452794.1:c.4694T=	XP_024308562.1:p.Val1565=
XM_024452795.1:c.4694T=	XP_024308563.1:p.Val1565=
NM_001371271.1:c.4694T=	NP_001358200.1:p.Val1565=
NM_001374353.1:c.4643T= MANE Select	NP_001361282.1:p.Val1548=
NM_001374354.1:c.4268T=	NP_001361283.1:p.Val1423=
NM_005270.5:c.4694T=	NP_005261.2:p.Val1565=