Canonical Allele Identifier: CA428229973

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121736138C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120978562C>A , CM000664.2:g.120978562C>A	GRCh38
NC_000002.11:g.121736138C>A , CM000664.1:g.121736138C>A	GRCh37
NC_000002.10:g.121452608C>A	NCBI36
NG_009030.1:g.186272C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.1446C>A MANE Select	ENSP00000354586.5:p.Gly482=
ENST00000452319.6:c.1497C>A	ENSP00000390436.1:p.Gly499=
ENST00000314490.15:c.510C>A	ENSP00000312694.12:p.Gly170=
ENST00000341310.10:c.*545C>A	ENSP00000344473.6:n.*545C>A
ENST00000361492.8:c.1497C>A	ENSP00000354586.4:p.Gly499=
ENST00000435313.6:n.1471C>A
ENST00000437950.5:c.*596C>A	ENSP00000415773.1:n.*596C>A
ENST00000438299.5:c.*596C>A	ENSP00000400593.1:n.*596C>A
ENST00000445186.5:c.*596C>A	ENSP00000397488.1:n.*596C>A
ENST00000452319.5:c.1497C>A	ENSP00000390436.1:p.Gly499=
ENST00000452692.5:c.*545C>A	ENSP00000403715.1:n.*545C>A
NM_005270.4:c.1497C>A	NP_005261.2:p.Gly499=
XM_006712422.1:c.1446C>A	XP_006712485.1:p.Gly482=
XM_011510969.1:c.1479C>A	XP_011509271.1:p.Gly493=
XM_011510970.1:c.1356C>A	XP_011509272.1:p.Gly452=
XM_011510971.1:c.1302C>A	XP_011509273.1:p.Gly434=
XM_011510972.1:c.1302C>A	XP_011509274.1:p.Gly434=
XM_011510973.1:c.1122C>A	XP_011509275.1:p.Gly374=
XM_011510974.1:c.1071C>A	XP_011509276.1:p.Gly357=
XM_006712422.3:c.1446C>A	XP_006712485.1:p.Gly482=
XM_011510969.2:c.1749C>A	XP_011509271.2:p.Gly583=
XM_011510970.2:c.1356C>A	XP_011509272.1:p.Gly452=
XM_011510971.2:c.1302C>A	XP_011509273.1:p.Gly434=
XM_011510972.2:c.1398C>A	XP_011509274.2:p.Gly466=
XM_011510973.2:c.1122C>A	XP_011509275.1:p.Gly374=
XM_011510974.2:c.1071C>A	XP_011509276.1:p.Gly357=
XM_017003818.1:c.1698C>A	XP_016859307.1:p.Gly566=
XM_024452794.1:c.1497C>A	XP_024308562.1:p.Gly499=
XM_024452795.1:c.1497C>A	XP_024308563.1:p.Gly499=
NM_001371271.1:c.1497C>A	NP_001358200.1:p.Gly499=
NM_001374353.1:c.1446C>A MANE Select	NP_001361282.1:p.Gly482=
NM_001374354.1:c.1071C>A	NP_001361283.1:p.Gly357=
NM_005270.5:c.1497C>A	NP_005261.2:p.Gly499=