Canonical Allele Identifier: CA1283796212

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990639C= , CM000664.2:g.120990639C=	GRCh38
NC_000002.11:g.121748215C= , CM000664.1:g.121748215C=	GRCh37
NC_000002.10:g.121464685C=	NCBI36
NG_009030.1:g.198349C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4674C= MANE Select	ENSP00000354586.5:p.Leu1558=
ENST00000452319.6:c.4725C=	ENSP00000390436.1:p.Leu1575=
ENST00000341310.10:c.*3773C=	ENSP00000344473.6:n.*3773C=
ENST00000361492.8:c.4725C=	ENSP00000354586.4:p.Leu1575=
ENST00000438299.5:c.*2593C=	ENSP00000400593.1:n.*2593C=
ENST00000445186.5:c.*3824C=	ENSP00000397488.1:n.*3824C=
ENST00000452319.5:c.4725C=	ENSP00000390436.1:p.Leu1575=
ENST00000452692.5:c.*2542C=	ENSP00000403715.1:n.*2542C=
NM_005270.4:c.4725C=	NP_005261.2:p.Leu1575=
XM_006712422.1:c.4674C=	XP_006712485.1:p.Leu1558=
XM_011510969.1:c.4707C=	XP_011509271.1:p.Leu1569=
XM_011510970.1:c.4584C=	XP_011509272.1:p.Leu1528=
XM_011510971.1:c.4530C=	XP_011509273.1:p.Leu1510=
XM_011510972.1:c.4530C=	XP_011509274.1:p.Leu1510=
XM_011510973.1:c.4350C=	XP_011509275.1:p.Leu1450=
XM_011510974.1:c.4299C=	XP_011509276.1:p.Leu1433=
XM_006712422.3:c.4674C=	XP_006712485.1:p.Leu1558=
XM_011510969.2:c.4977C=	XP_011509271.2:p.Leu1659=
XM_011510970.2:c.4584C=	XP_011509272.1:p.Leu1528=
XM_011510971.2:c.4530C=	XP_011509273.1:p.Leu1510=
XM_011510972.2:c.4626C=	XP_011509274.2:p.Leu1542=
XM_011510973.2:c.4350C=	XP_011509275.1:p.Leu1450=
XM_011510974.2:c.4299C=	XP_011509276.1:p.Leu1433=
XM_017003818.1:c.4926C=	XP_016859307.1:p.Leu1642=
XM_024452794.1:c.4725C=	XP_024308562.1:p.Leu1575=
XM_024452795.1:c.4725C=	XP_024308563.1:p.Leu1575=
NM_001371271.1:c.4725C=	NP_001358200.1:p.Leu1575=
NM_001374353.1:c.4674C= MANE Select	NP_001361282.1:p.Leu1558=
NM_001374354.1:c.4299C=	NP_001361283.1:p.Leu1433=
NM_005270.5:c.4725C=	NP_005261.2:p.Leu1575=