Canonical Allele Identifier: CA1283790677

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120978512C= , CM000664.2:g.120978512C=	GRCh38
NC_000002.11:g.121736088C= , CM000664.1:g.121736088C=	GRCh37
NC_000002.10:g.121452558C=	NCBI36
NG_009030.1:g.186222C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.1396C= MANE Select	ENSP00000354586.5:p.Pro466=
ENST00000452319.6:c.1447C=	ENSP00000390436.1:p.Pro483=
ENST00000314490.15:c.460C=	ENSP00000312694.12:p.Pro154=
ENST00000341310.10:c.*495C=	ENSP00000344473.6:n.*495C=
ENST00000361492.8:c.1447C=	ENSP00000354586.4:p.Pro483=
ENST00000435313.6:n.1421C=
ENST00000437950.5:c.*546C=	ENSP00000415773.1:n.*546C=
ENST00000438299.5:c.*546C=	ENSP00000400593.1:n.*546C=
ENST00000445186.5:c.*546C=	ENSP00000397488.1:n.*546C=
ENST00000452319.5:c.1447C=	ENSP00000390436.1:p.Pro483=
ENST00000452692.5:c.*495C=	ENSP00000403715.1:n.*495C=
NM_005270.4:c.1447C=	NP_005261.2:p.Pro483=
XM_006712422.1:c.1396C=	XP_006712485.1:p.Pro466=
XM_011510969.1:c.1429C=	XP_011509271.1:p.Pro477=
XM_011510970.1:c.1306C=	XP_011509272.1:p.Pro436=
XM_011510971.1:c.1252C=	XP_011509273.1:p.Pro418=
XM_011510972.1:c.1252C=	XP_011509274.1:p.Pro418=
XM_011510973.1:c.1072C=	XP_011509275.1:p.Pro358=
XM_011510974.1:c.1021C=	XP_011509276.1:p.Pro341=
XM_006712422.3:c.1396C=	XP_006712485.1:p.Pro466=
XM_011510969.2:c.1699C=	XP_011509271.2:p.Pro567=
XM_011510970.2:c.1306C=	XP_011509272.1:p.Pro436=
XM_011510971.2:c.1252C=	XP_011509273.1:p.Pro418=
XM_011510972.2:c.1348C=	XP_011509274.2:p.Pro450=
XM_011510973.2:c.1072C=	XP_011509275.1:p.Pro358=
XM_011510974.2:c.1021C=	XP_011509276.1:p.Pro341=
XM_017003818.1:c.1648C=	XP_016859307.1:p.Pro550=
XM_024452794.1:c.1447C=	XP_024308562.1:p.Pro483=
XM_024452795.1:c.1447C=	XP_024308563.1:p.Pro483=
NM_001371271.1:c.1447C=	NP_001358200.1:p.Pro483=
NM_001374353.1:c.1396C= MANE Select	NP_001361282.1:p.Pro466=
NM_001374354.1:c.1021C=	NP_001361283.1:p.Pro341=
NM_005270.5:c.1447C=	NP_005261.2:p.Pro483=