Canonical Allele Identifier: CA428559481

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121748182T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990606T>G , CM000664.2:g.120990606T>G	GRCh38
NC_000002.11:g.121748182T>G , CM000664.1:g.121748182T>G	GRCh37
NC_000002.10:g.121464652T>G	NCBI36
NG_009030.1:g.198316T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4641T>G MANE Select	ENSP00000354586.5:p.Ala1547=
ENST00000452319.6:c.4692T>G	ENSP00000390436.1:p.Ala1564=
ENST00000341310.10:c.*3740T>G	ENSP00000344473.6:n.*3740T>G
ENST00000361492.8:c.4692T>G	ENSP00000354586.4:p.Ala1564=
ENST00000438299.5:c.*2560T>G	ENSP00000400593.1:n.*2560T>G
ENST00000445186.5:c.*3791T>G	ENSP00000397488.1:n.*3791T>G
ENST00000452319.5:c.4692T>G	ENSP00000390436.1:p.Ala1564=
ENST00000452692.5:c.*2509T>G	ENSP00000403715.1:n.*2509T>G
NM_005270.4:c.4692T>G	NP_005261.2:p.Ala1564=
XM_006712422.1:c.4641T>G	XP_006712485.1:p.Ala1547=
XM_011510969.1:c.4674T>G	XP_011509271.1:p.Ala1558=
XM_011510970.1:c.4551T>G	XP_011509272.1:p.Ala1517=
XM_011510971.1:c.4497T>G	XP_011509273.1:p.Ala1499=
XM_011510972.1:c.4497T>G	XP_011509274.1:p.Ala1499=
XM_011510973.1:c.4317T>G	XP_011509275.1:p.Ala1439=
XM_011510974.1:c.4266T>G	XP_011509276.1:p.Ala1422=
XM_006712422.3:c.4641T>G	XP_006712485.1:p.Ala1547=
XM_011510969.2:c.4944T>G	XP_011509271.2:p.Ala1648=
XM_011510970.2:c.4551T>G	XP_011509272.1:p.Ala1517=
XM_011510971.2:c.4497T>G	XP_011509273.1:p.Ala1499=
XM_011510972.2:c.4593T>G	XP_011509274.2:p.Ala1531=
XM_011510973.2:c.4317T>G	XP_011509275.1:p.Ala1439=
XM_011510974.2:c.4266T>G	XP_011509276.1:p.Ala1422=
XM_017003818.1:c.4893T>G	XP_016859307.1:p.Ala1631=
XM_024452794.1:c.4692T>G	XP_024308562.1:p.Ala1564=
XM_024452795.1:c.4692T>G	XP_024308563.1:p.Ala1564=
NM_001371271.1:c.4692T>G	NP_001358200.1:p.Ala1564=
NM_001374353.1:c.4641T>G MANE Select	NP_001361282.1:p.Ala1547=
NM_001374354.1:c.4266T>G	NP_001361283.1:p.Ala1422=
NM_005270.5:c.4692T>G	NP_005261.2:p.Ala1564=