Canonical Allele Identifier: CA428750707

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121748083C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990507C>A , CM000664.2:g.120990507C>A	GRCh38
NC_000002.11:g.121748083C>A , CM000664.1:g.121748083C>A	GRCh37
NC_000002.10:g.121464553C>A	NCBI36
NG_009030.1:g.198217C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4542C>A MANE Select	ENSP00000354586.5:p.Pro1514=
ENST00000452319.6:c.4593C>A	ENSP00000390436.1:p.Pro1531=
ENST00000341310.10:c.*3641C>A	ENSP00000344473.6:n.*3641C>A
ENST00000361492.8:c.4593C>A	ENSP00000354586.4:p.Pro1531=
ENST00000438299.5:c.*2544-83C>A	ENSP00000400593.1:n.*2544-83C>A
ENST00000445186.5:c.*3692C>A	ENSP00000397488.1:n.*3692C>A
ENST00000452319.5:c.4593C>A	ENSP00000390436.1:p.Pro1531=
ENST00000452692.5:c.*2493-83C>A	ENSP00000403715.1:n.*2493-83C>A
NM_005270.4:c.4593C>A	NP_005261.2:p.Pro1531=
XM_006712422.1:c.4542C>A	XP_006712485.1:p.Pro1514=
XM_011510969.1:c.4575C>A	XP_011509271.1:p.Pro1525=
XM_011510970.1:c.4452C>A	XP_011509272.1:p.Pro1484=
XM_011510971.1:c.4398C>A	XP_011509273.1:p.Pro1466=
XM_011510972.1:c.4398C>A	XP_011509274.1:p.Pro1466=
XM_011510973.1:c.4218C>A	XP_011509275.1:p.Pro1406=
XM_011510974.1:c.4167C>A	XP_011509276.1:p.Pro1389=
XM_006712422.3:c.4542C>A	XP_006712485.1:p.Pro1514=
XM_011510969.2:c.4845C>A	XP_011509271.2:p.Pro1615=
XM_011510970.2:c.4452C>A	XP_011509272.1:p.Pro1484=
XM_011510971.2:c.4398C>A	XP_011509273.1:p.Pro1466=
XM_011510972.2:c.4494C>A	XP_011509274.2:p.Pro1498=
XM_011510973.2:c.4218C>A	XP_011509275.1:p.Pro1406=
XM_011510974.2:c.4167C>A	XP_011509276.1:p.Pro1389=
XM_017003818.1:c.4794C>A	XP_016859307.1:p.Pro1598=
XM_024452794.1:c.4593C>A	XP_024308562.1:p.Pro1531=
XM_024452795.1:c.4593C>A	XP_024308563.1:p.Pro1531=
NM_001371271.1:c.4593C>A	NP_001358200.1:p.Pro1531=
NM_001374353.1:c.4542C>A MANE Select	NP_001361282.1:p.Pro1514=
NM_001374354.1:c.4167C>A	NP_001361283.1:p.Pro1389=
NM_005270.5:c.4593C>A	NP_005261.2:p.Pro1531=