Canonical Allele Identifier: CA201053

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990246G>A , CM000664.2:g.120990246G>A	GRCh38
NC_000002.11:g.121747822G>A , CM000664.1:g.121747822G>A	GRCh37
NC_000002.10:g.121464292G>A	NCBI36
NG_009030.1:g.197956G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4281G>A MANE Select	ENSP00000354586.5:p.Met1427Ile
ENST00000452319.6:c.4332G>A	ENSP00000390436.1:p.Met1444Ile
ENST00000341310.10:c.*3380G>A	ENSP00000344473.6:n.*3380G>A
ENST00000361492.8:c.4332G>A	ENSP00000354586.4:p.Met1444Ile
ENST00000438299.5:c.*2544-344G>A	ENSP00000400593.1:n.*2544-344G>A
ENST00000445186.5:c.*3431G>A	ENSP00000397488.1:n.*3431G>A
ENST00000452319.5:c.4332G>A	ENSP00000390436.1:p.Met1444Ile
ENST00000452692.5:c.*2493-344G>A	ENSP00000403715.1:n.*2493-344G>A
NM_005270.4:c.4332G>A	NP_005261.2:p.Met1444Ile
XM_006712422.1:c.4281G>A	XP_006712485.1:p.Met1427Ile
XM_011510969.1:c.4314G>A	XP_011509271.1:p.Met1438Ile
XM_011510970.1:c.4191G>A	XP_011509272.1:p.Met1397Ile
XM_011510971.1:c.4137G>A	XP_011509273.1:p.Met1379Ile
XM_011510972.1:c.4137G>A	XP_011509274.1:p.Met1379Ile
XM_011510973.1:c.3957G>A	XP_011509275.1:p.Met1319Ile
XM_011510974.1:c.3906G>A	XP_011509276.1:p.Met1302Ile
XM_006712422.3:c.4281G>A	XP_006712485.1:p.Met1427Ile
XM_011510969.2:c.4584G>A	XP_011509271.2:p.Met1528Ile
XM_011510970.2:c.4191G>A	XP_011509272.1:p.Met1397Ile
XM_011510971.2:c.4137G>A	XP_011509273.1:p.Met1379Ile
XM_011510972.2:c.4233G>A	XP_011509274.2:p.Met1411Ile
XM_011510973.2:c.3957G>A	XP_011509275.1:p.Met1319Ile
XM_011510974.2:c.3906G>A	XP_011509276.1:p.Met1302Ile
XM_017003818.1:c.4533G>A	XP_016859307.1:p.Met1511Ile
XM_024452794.1:c.4332G>A	XP_024308562.1:p.Met1444Ile
XM_024452795.1:c.4332G>A	XP_024308563.1:p.Met1444Ile
NM_001371271.1:c.4332G>A	NP_001358200.1:p.Met1444Ile
NM_001374353.1:c.4281G>A MANE Select	NP_001361282.1:p.Met1427Ile
NM_001374354.1:c.3906G>A	NP_001361283.1:p.Met1302Ile
NM_005270.5:c.4332G>A	NP_005261.2:p.Met1444Ile