Canonical Allele Identifier: CA1283795458

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120989088C= , CM000664.2:g.120989088C=	GRCh38
NC_000002.11:g.121746664C= , CM000664.1:g.121746664C=	GRCh37
NC_000002.10:g.121463134C=	NCBI36
NG_009030.1:g.196798C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361492.9:c.3123C= MANE Select	ENSP00000354586.5:p.Asp1041=
ENST00000452319.6:c.3174C=	ENSP00000390436.1:p.Asp1058=
ENST00000341310.10:c.*2222C=	ENSP00000344473.6:n.*2222C=
ENST00000361492.8:c.3174C=	ENSP00000354586.4:p.Asp1058=
ENST00000438299.5:c.*2273C=	ENSP00000400593.1:n.*2273C=
ENST00000445186.5:c.*2273C=	ENSP00000397488.1:n.*2273C=
ENST00000452319.5:c.3174C=	ENSP00000390436.1:p.Asp1058=
ENST00000452692.5:c.*2222C=	ENSP00000403715.1:n.*2222C=
NM_005270.4:c.3174C=	NP_005261.2:p.Asp1058=
XM_006712422.1:c.3123C=	XP_006712485.1:p.Asp1041=
XM_011510969.1:c.3156C=	XP_011509271.1:p.Asp1052=
XM_011510970.1:c.3033C=	XP_011509272.1:p.Asp1011=
XM_011510971.1:c.2979C=	XP_011509273.1:p.Asp993=
XM_011510972.1:c.2979C=	XP_011509274.1:p.Asp993=
XM_011510973.1:c.2799C=	XP_011509275.1:p.Asp933=
XM_011510974.1:c.2748C=	XP_011509276.1:p.Asp916=
XM_006712422.3:c.3123C=	XP_006712485.1:p.Asp1041=
XM_011510969.2:c.3426C=	XP_011509271.2:p.Asp1142=
XM_011510970.2:c.3033C=	XP_011509272.1:p.Asp1011=
XM_011510971.2:c.2979C=	XP_011509273.1:p.Asp993=
XM_011510972.2:c.3075C=	XP_011509274.2:p.Asp1025=
XM_011510973.2:c.2799C=	XP_011509275.1:p.Asp933=
XM_011510974.2:c.2748C=	XP_011509276.1:p.Asp916=
XM_017003818.1:c.3375C=	XP_016859307.1:p.Asp1125=
XM_024452794.1:c.3174C=	XP_024308562.1:p.Asp1058=
XM_024452795.1:c.3174C=	XP_024308563.1:p.Asp1058=
NM_001371271.1:c.3174C=	NP_001358200.1:p.Asp1058=
NM_001374353.1:c.3123C= MANE Select	NP_001361282.1:p.Asp1041=
NM_001374354.1:c.2748C=	NP_001361283.1:p.Asp916=
NM_005270.5:c.3174C=	NP_005261.2:p.Asp1058=