Canonical Allele Identifier: CA428749711

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121746661G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120989085G>A , CM000664.2:g.120989085G>A	GRCh38
NC_000002.11:g.121746661G>A , CM000664.1:g.121746661G>A	GRCh37
NC_000002.10:g.121463131G>A	NCBI36
NG_009030.1:g.196795G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361492.9:c.3120G>A MANE Select	ENSP00000354586.5:p.Glu1040=
ENST00000452319.6:c.3171G>A	ENSP00000390436.1:p.Glu1057=
ENST00000341310.10:c.*2219G>A	ENSP00000344473.6:n.*2219G>A
ENST00000361492.8:c.3171G>A	ENSP00000354586.4:p.Glu1057=
ENST00000438299.5:c.*2270G>A	ENSP00000400593.1:n.*2270G>A
ENST00000445186.5:c.*2270G>A	ENSP00000397488.1:n.*2270G>A
ENST00000452319.5:c.3171G>A	ENSP00000390436.1:p.Glu1057=
ENST00000452692.5:c.*2219G>A	ENSP00000403715.1:n.*2219G>A
NM_005270.4:c.3171G>A	NP_005261.2:p.Glu1057=
XM_006712422.1:c.3120G>A	XP_006712485.1:p.Glu1040=
XM_011510969.1:c.3153G>A	XP_011509271.1:p.Glu1051=
XM_011510970.1:c.3030G>A	XP_011509272.1:p.Glu1010=
XM_011510971.1:c.2976G>A	XP_011509273.1:p.Glu992=
XM_011510972.1:c.2976G>A	XP_011509274.1:p.Glu992=
XM_011510973.1:c.2796G>A	XP_011509275.1:p.Glu932=
XM_011510974.1:c.2745G>A	XP_011509276.1:p.Glu915=
XM_006712422.3:c.3120G>A	XP_006712485.1:p.Glu1040=
XM_011510969.2:c.3423G>A	XP_011509271.2:p.Glu1141=
XM_011510970.2:c.3030G>A	XP_011509272.1:p.Glu1010=
XM_011510971.2:c.2976G>A	XP_011509273.1:p.Glu992=
XM_011510972.2:c.3072G>A	XP_011509274.2:p.Glu1024=
XM_011510973.2:c.2796G>A	XP_011509275.1:p.Glu932=
XM_011510974.2:c.2745G>A	XP_011509276.1:p.Glu915=
XM_017003818.1:c.3372G>A	XP_016859307.1:p.Glu1124=
XM_024452794.1:c.3171G>A	XP_024308562.1:p.Glu1057=
XM_024452795.1:c.3171G>A	XP_024308563.1:p.Glu1057=
NM_001371271.1:c.3171G>A	NP_001358200.1:p.Glu1057=
NM_001374353.1:c.3120G>A MANE Select	NP_001361282.1:p.Glu1040=
NM_001374354.1:c.2745G>A	NP_001361283.1:p.Glu915=
NM_005270.5:c.3171G>A	NP_005261.2:p.Glu1057=