Canonical Allele Identifier: CA348180234
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990595A>G , CM000664.2:g.120990595A>G GRCh38
NC_000002.11:g.121748171A>G , CM000664.1:g.121748171A>G GRCh37
NC_000002.10:g.121464641A>G NCBI36
NG_009030.1:g.198305A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4630A>G MANE Select ENSP00000354586.5:p.Ser1544Gly
ENST00000452319.6:c.4681A>G ENSP00000390436.1:p.Ser1561Gly
ENST00000341310.10:c.*3729A>G ENSP00000344473.6:n.*3729A>G
ENST00000361492.8:c.4681A>G ENSP00000354586.4:p.Ser1561Gly
ENST00000438299.5:c.*2549A>G ENSP00000400593.1:n.*2549A>G
ENST00000445186.5:c.*3780A>G ENSP00000397488.1:n.*3780A>G
ENST00000452319.5:c.4681A>G ENSP00000390436.1:p.Ser1561Gly
ENST00000452692.5:c.*2498A>G ENSP00000403715.1:n.*2498A>G
NM_005270.4:c.4681A>G NP_005261.2:p.Ser1561Gly
XM_006712422.1:c.4630A>G XP_006712485.1:p.Ser1544Gly
XM_011510969.1:c.4663A>G XP_011509271.1:p.Ser1555Gly
XM_011510970.1:c.4540A>G XP_011509272.1:p.Ser1514Gly
XM_011510971.1:c.4486A>G XP_011509273.1:p.Ser1496Gly
XM_011510972.1:c.4486A>G XP_011509274.1:p.Ser1496Gly
XM_011510973.1:c.4306A>G XP_011509275.1:p.Ser1436Gly
XM_011510974.1:c.4255A>G XP_011509276.1:p.Ser1419Gly
XM_006712422.3:c.4630A>G XP_006712485.1:p.Ser1544Gly
XM_011510969.2:c.4933A>G XP_011509271.2:p.Ser1645Gly
XM_011510970.2:c.4540A>G XP_011509272.1:p.Ser1514Gly
XM_011510971.2:c.4486A>G XP_011509273.1:p.Ser1496Gly
XM_011510972.2:c.4582A>G XP_011509274.2:p.Ser1528Gly
XM_011510973.2:c.4306A>G XP_011509275.1:p.Ser1436Gly
XM_011510974.2:c.4255A>G XP_011509276.1:p.Ser1419Gly
XM_017003818.1:c.4882A>G XP_016859307.1:p.Ser1628Gly
XM_024452794.1:c.4681A>G XP_024308562.1:p.Ser1561Gly
XM_024452795.1:c.4681A>G XP_024308563.1:p.Ser1561Gly
NM_001371271.1:c.4681A>G NP_001358200.1:p.Ser1561Gly
NM_001374353.1:c.4630A>G MANE Select NP_001361282.1:p.Ser1544Gly
NM_001374354.1:c.4255A>G NP_001361283.1:p.Ser1419Gly
NM_005270.5:c.4681A>G NP_005261.2:p.Ser1561Gly