Canonical Allele Identifier: CA1283796162

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990533A= , CM000664.2:g.120990533A=	GRCh38
NC_000002.11:g.121748109A= , CM000664.1:g.121748109A=	GRCh37
NC_000002.10:g.121464579A=	NCBI36
NG_009030.1:g.198243A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4568A= MANE Select	ENSP00000354586.5:p.Asn1523=
ENST00000452319.6:c.4619A=	ENSP00000390436.1:p.Asn1540=
ENST00000341310.10:c.*3667A=	ENSP00000344473.6:n.*3667A=
ENST00000361492.8:c.4619A=	ENSP00000354586.4:p.Asn1540=
ENST00000438299.5:c.*2544-57A=	ENSP00000400593.1:n.*2544-57A=
ENST00000445186.5:c.*3718A=	ENSP00000397488.1:n.*3718A=
ENST00000452319.5:c.4619A=	ENSP00000390436.1:p.Asn1540=
ENST00000452692.5:c.*2493-57A=	ENSP00000403715.1:n.*2493-57A=
NM_005270.4:c.4619A=	NP_005261.2:p.Asn1540=
XM_006712422.1:c.4568A=	XP_006712485.1:p.Asn1523=
XM_011510969.1:c.4601A=	XP_011509271.1:p.Asn1534=
XM_011510970.1:c.4478A=	XP_011509272.1:p.Asn1493=
XM_011510971.1:c.4424A=	XP_011509273.1:p.Asn1475=
XM_011510972.1:c.4424A=	XP_011509274.1:p.Asn1475=
XM_011510973.1:c.4244A=	XP_011509275.1:p.Asn1415=
XM_011510974.1:c.4193A=	XP_011509276.1:p.Asn1398=
XM_006712422.3:c.4568A=	XP_006712485.1:p.Asn1523=
XM_011510969.2:c.4871A=	XP_011509271.2:p.Asn1624=
XM_011510970.2:c.4478A=	XP_011509272.1:p.Asn1493=
XM_011510971.2:c.4424A=	XP_011509273.1:p.Asn1475=
XM_011510972.2:c.4520A=	XP_011509274.2:p.Asn1507=
XM_011510973.2:c.4244A=	XP_011509275.1:p.Asn1415=
XM_011510974.2:c.4193A=	XP_011509276.1:p.Asn1398=
XM_017003818.1:c.4820A=	XP_016859307.1:p.Asn1607=
XM_024452794.1:c.4619A=	XP_024308562.1:p.Asn1540=
XM_024452795.1:c.4619A=	XP_024308563.1:p.Asn1540=
NM_001371271.1:c.4619A=	NP_001358200.1:p.Asn1540=
NM_001374353.1:c.4568A= MANE Select	NP_001361282.1:p.Asn1523=
NM_001374354.1:c.4193A=	NP_001361283.1:p.Asn1398=
NM_005270.5:c.4619A=	NP_005261.2:p.Asn1540=