Canonical Allele Identifier: CA1283790723

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120978618_120978619delinsCA , CM000664.2:g.120978618_120978619delinsCA	GRCh38
NC_000002.11:g.121736194_121736195delinsCA , CM000664.1:g.121736194_121736195delinsCA	GRCh37
NC_000002.10:g.121452664_121452665delinsCA	NCBI36
NG_009030.1:g.186328_186329delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.1467+35_1467+36delinsCA MANE Select	ENSP00000354586.5:n.1467+35_1467+36delinsCA
ENST00000452319.6:c.1518+35_1518+36delinsCA	ENSP00000390436.1:n.1518+35_1518+36delinsCA
ENST00000314490.15:c.531+35_531+36delinsCA	ENSP00000312694.12:n.531+35_531+36delinsCA
ENST00000341310.10:c.*566+35_*566+36delinsCA	ENSP00000344473.6:n.*566+35_*566+36delinsCA
ENST00000361492.8:c.1518+35_1518+36delinsCA	ENSP00000354586.4:n.1518+35_1518+36delinsCA
ENST00000435313.6:n.1492+35_1492+36delinsCA
ENST00000437950.5:c.*617+35_*617+36delinsCA	ENSP00000415773.1:n.*617+35_*617+36delinsCA
ENST00000438299.5:c.*617+35_*617+36delinsCA	ENSP00000400593.1:n.*617+35_*617+36delinsCA
ENST00000445186.5:c.*617+35_*617+36delinsCA	ENSP00000397488.1:n.*617+35_*617+36delinsCA
ENST00000452319.5:c.1518+35_1518+36delinsCA	ENSP00000390436.1:n.1518+35_1518+36delinsCA
ENST00000452692.5:c.*566+35_*566+36delinsCA	ENSP00000403715.1:n.*566+35_*566+36delinsCA
NM_005270.4:c.1518+35_1518+36delinsCA	NP_005261.2:n.1518+35_1518+36delinsCA
XM_006712422.1:c.1467+35_1467+36delinsCA	XP_006712485.1:n.1467+35_1467+36delinsCA
XM_011510969.1:c.1500+35_1500+36delinsCA	XP_011509271.1:n.1500+35_1500+36delinsCA
XM_011510970.1:c.1377+35_1377+36delinsCA	XP_011509272.1:n.1377+35_1377+36delinsCA
XM_011510971.1:c.1323+35_1323+36delinsCA	XP_011509273.1:n.1323+35_1323+36delinsCA
XM_011510972.1:c.1323+35_1323+36delinsCA	XP_011509274.1:n.1323+35_1323+36delinsCA
XM_011510973.1:c.1143+35_1143+36delinsCA	XP_011509275.1:n.1143+35_1143+36delinsCA
XM_011510974.1:c.1092+35_1092+36delinsCA	XP_011509276.1:n.1092+35_1092+36delinsCA
XM_006712422.3:c.1467+35_1467+36delinsCA	XP_006712485.1:n.1467+35_1467+36delinsCA
XM_011510969.2:c.1770+35_1770+36delinsCA	XP_011509271.2:n.1770+35_1770+36delinsCA
XM_011510970.2:c.1377+35_1377+36delinsCA	XP_011509272.1:n.1377+35_1377+36delinsCA
XM_011510971.2:c.1323+35_1323+36delinsCA	XP_011509273.1:n.1323+35_1323+36delinsCA
XM_011510972.2:c.1419+35_1419+36delinsCA	XP_011509274.2:n.1419+35_1419+36delinsCA
XM_011510973.2:c.1143+35_1143+36delinsCA	XP_011509275.1:n.1143+35_1143+36delinsCA
XM_011510974.2:c.1092+35_1092+36delinsCA	XP_011509276.1:n.1092+35_1092+36delinsCA
XM_017003818.1:c.1719+35_1719+36delinsCA	XP_016859307.1:n.1719+35_1719+36delinsCA
XM_024452794.1:c.1518+35_1518+36delinsCA	XP_024308562.1:n.1518+35_1518+36delinsCA
XM_024452795.1:c.1518+35_1518+36delinsCA	XP_024308563.1:n.1518+35_1518+36delinsCA
NM_001371271.1:c.1518+35_1518+36delinsCA	NP_001358200.1:n.1518+35_1518+36delinsCA
NM_001374353.1:c.1467+35_1467+36delinsCA MANE Select	NP_001361282.1:n.1467+35_1467+36delinsCA
NM_001374354.1:c.1092+35_1092+36delinsCA	NP_001361283.1:n.1092+35_1092+36delinsCA
NM_005270.5:c.1518+35_1518+36delinsCA	NP_005261.2:n.1518+35_1518+36delinsCA