Canonical Allele Identifier: CA1283790544

Gene: GLI2

Linked Data

• dbSNP Id: rs1682552133

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120978240_120978249del , CM000664.2:g.120978240_120978249del	GRCh38
NC_000002.11:g.121735816_121735825del , CM000664.1:g.121735816_121735825del	GRCh37
NC_000002.10:g.121452286_121452295del	NCBI36
NG_009030.1:g.185950_185959del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.1318-194_1318-185del MANE Select	ENSP00000354586.5:n.1318-194_1318-185del
ENST00000452319.6:c.1369-194_1369-185del	ENSP00000390436.1:n.1369-194_1369-185del
ENST00000314490.15:c.382-194_382-185del	ENSP00000312694.12:n.382-194_382-185del
ENST00000341310.10:c.*417-194_*417-185del	ENSP00000344473.6:n.*417-194_*417-185del
ENST00000361492.8:c.1369-194_1369-185del	ENSP00000354586.4:n.1369-194_1369-185del
ENST00000435313.6:n.1343-194_1343-185del
ENST00000437950.5:c.*468-194_*468-185del	ENSP00000415773.1:n.*468-194_*468-185del
ENST00000438299.5:c.*468-194_*468-185del	ENSP00000400593.1:n.*468-194_*468-185del
ENST00000445186.5:c.*468-194_*468-185del	ENSP00000397488.1:n.*468-194_*468-185del
ENST00000452319.5:c.1369-194_1369-185del	ENSP00000390436.1:n.1369-194_1369-185del
ENST00000452692.5:c.*417-194_*417-185del	ENSP00000403715.1:n.*417-194_*417-185del
NM_005270.4:c.1369-194_1369-185del	NP_005261.2:n.1369-194_1369-185del
XM_006712422.1:c.1318-194_1318-185del	XP_006712485.1:n.1318-194_1318-185del
XM_011510969.1:c.1351-194_1351-185del	XP_011509271.1:n.1351-194_1351-185del
XM_011510970.1:c.1228-194_1228-185del	XP_011509272.1:n.1228-194_1228-185del
XM_011510971.1:c.1174-194_1174-185del	XP_011509273.1:n.1174-194_1174-185del
XM_011510972.1:c.1174-194_1174-185del	XP_011509274.1:n.1174-194_1174-185del
XM_011510973.1:c.994-194_994-185del	XP_011509275.1:n.994-194_994-185del
XM_011510974.1:c.943-194_943-185del	XP_011509276.1:n.943-194_943-185del
XM_006712422.3:c.1318-194_1318-185del	XP_006712485.1:n.1318-194_1318-185del
XM_011510969.2:c.1621-194_1621-185del	XP_011509271.2:n.1621-194_1621-185del
XM_011510970.2:c.1228-194_1228-185del	XP_011509272.1:n.1228-194_1228-185del
XM_011510971.2:c.1174-194_1174-185del	XP_011509273.1:n.1174-194_1174-185del
XM_011510972.2:c.1270-194_1270-185del	XP_011509274.2:n.1270-194_1270-185del
XM_011510973.2:c.994-194_994-185del	XP_011509275.1:n.994-194_994-185del
XM_011510974.2:c.943-194_943-185del	XP_011509276.1:n.943-194_943-185del
XM_017003818.1:c.1570-194_1570-185del	XP_016859307.1:n.1570-194_1570-185del
XM_024452794.1:c.1369-194_1369-185del	XP_024308562.1:n.1369-194_1369-185del
XM_024452795.1:c.1369-194_1369-185del	XP_024308563.1:n.1369-194_1369-185del
NM_001371271.1:c.1369-194_1369-185del	NP_001358200.1:n.1369-194_1369-185del
NM_001374353.1:c.1318-194_1318-185del MANE Select	NP_001361282.1:n.1318-194_1318-185del
NM_001374354.1:c.943-194_943-185del	NP_001361283.1:n.943-194_943-185del
NM_005270.5:c.1369-194_1369-185del	NP_005261.2:n.1369-194_1369-185del