Canonical Allele Identifier: CA1283790700

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120978582C= , CM000664.2:g.120978582C=	GRCh38
NC_000002.11:g.121736158C= , CM000664.1:g.121736158C=	GRCh37
NC_000002.10:g.121452628C=	NCBI36
NG_009030.1:g.186292C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.1466C= MANE Select	ENSP00000354586.5:p.Thr489=
ENST00000452319.6:c.1517C=	ENSP00000390436.1:p.Thr506=
ENST00000314490.15:c.530C=	ENSP00000312694.12:p.Thr177=
ENST00000341310.10:c.*565C=	ENSP00000344473.6:n.*565C=
ENST00000361492.8:c.1517C=	ENSP00000354586.4:p.Thr506=
ENST00000435313.6:n.1491C=
ENST00000437950.5:c.*616C=	ENSP00000415773.1:n.*616C=
ENST00000438299.5:c.*616C=	ENSP00000400593.1:n.*616C=
ENST00000445186.5:c.*616C=	ENSP00000397488.1:n.*616C=
ENST00000452319.5:c.1517C=	ENSP00000390436.1:p.Thr506=
ENST00000452692.5:c.*565C=	ENSP00000403715.1:n.*565C=
NM_005270.4:c.1517C=	NP_005261.2:p.Thr506=
XM_006712422.1:c.1466C=	XP_006712485.1:p.Thr489=
XM_011510969.1:c.1499C=	XP_011509271.1:p.Thr500=
XM_011510970.1:c.1376C=	XP_011509272.1:p.Thr459=
XM_011510971.1:c.1322C=	XP_011509273.1:p.Thr441=
XM_011510972.1:c.1322C=	XP_011509274.1:p.Thr441=
XM_011510973.1:c.1142C=	XP_011509275.1:p.Thr381=
XM_011510974.1:c.1091C=	XP_011509276.1:p.Thr364=
XM_006712422.3:c.1466C=	XP_006712485.1:p.Thr489=
XM_011510969.2:c.1769C=	XP_011509271.2:p.Thr590=
XM_011510970.2:c.1376C=	XP_011509272.1:p.Thr459=
XM_011510971.2:c.1322C=	XP_011509273.1:p.Thr441=
XM_011510972.2:c.1418C=	XP_011509274.2:p.Thr473=
XM_011510973.2:c.1142C=	XP_011509275.1:p.Thr381=
XM_011510974.2:c.1091C=	XP_011509276.1:p.Thr364=
XM_017003818.1:c.1718C=	XP_016859307.1:p.Thr573=
XM_024452794.1:c.1517C=	XP_024308562.1:p.Thr506=
XM_024452795.1:c.1517C=	XP_024308563.1:p.Thr506=
NM_001371271.1:c.1517C=	NP_001358200.1:p.Thr506=
NM_001374353.1:c.1466C= MANE Select	NP_001361282.1:p.Thr489=
NM_001374354.1:c.1091C=	NP_001361283.1:p.Thr364=
NM_005270.5:c.1517C=	NP_005261.2:p.Thr506=