Canonical Allele Identifier: CA348180304
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990623C>G , CM000664.2:g.120990623C>G GRCh38
NC_000002.11:g.121748199C>G , CM000664.1:g.121748199C>G GRCh37
NC_000002.10:g.121464669C>G NCBI36
NG_009030.1:g.198333C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4658C>G MANE Select ENSP00000354586.5:p.Ser1553Cys
ENST00000452319.6:c.4709C>G ENSP00000390436.1:p.Ser1570Cys
ENST00000341310.10:c.*3757C>G ENSP00000344473.6:n.*3757C>G
ENST00000361492.8:c.4709C>G ENSP00000354586.4:p.Ser1570Cys
ENST00000438299.5:c.*2577C>G ENSP00000400593.1:n.*2577C>G
ENST00000445186.5:c.*3808C>G ENSP00000397488.1:n.*3808C>G
ENST00000452319.5:c.4709C>G ENSP00000390436.1:p.Ser1570Cys
ENST00000452692.5:c.*2526C>G ENSP00000403715.1:n.*2526C>G
NM_005270.4:c.4709C>G NP_005261.2:p.Ser1570Cys
XM_006712422.1:c.4658C>G XP_006712485.1:p.Ser1553Cys
XM_011510969.1:c.4691C>G XP_011509271.1:p.Ser1564Cys
XM_011510970.1:c.4568C>G XP_011509272.1:p.Ser1523Cys
XM_011510971.1:c.4514C>G XP_011509273.1:p.Ser1505Cys
XM_011510972.1:c.4514C>G XP_011509274.1:p.Ser1505Cys
XM_011510973.1:c.4334C>G XP_011509275.1:p.Ser1445Cys
XM_011510974.1:c.4283C>G XP_011509276.1:p.Ser1428Cys
XM_006712422.3:c.4658C>G XP_006712485.1:p.Ser1553Cys
XM_011510969.2:c.4961C>G XP_011509271.2:p.Ser1654Cys
XM_011510970.2:c.4568C>G XP_011509272.1:p.Ser1523Cys
XM_011510971.2:c.4514C>G XP_011509273.1:p.Ser1505Cys
XM_011510972.2:c.4610C>G XP_011509274.2:p.Ser1537Cys
XM_011510973.2:c.4334C>G XP_011509275.1:p.Ser1445Cys
XM_011510974.2:c.4283C>G XP_011509276.1:p.Ser1428Cys
XM_017003818.1:c.4910C>G XP_016859307.1:p.Ser1637Cys
XM_024452794.1:c.4709C>G XP_024308562.1:p.Ser1570Cys
XM_024452795.1:c.4709C>G XP_024308563.1:p.Ser1570Cys
NM_001371271.1:c.4709C>G NP_001358200.1:p.Ser1570Cys
NM_001374353.1:c.4658C>G MANE Select NP_001361282.1:p.Ser1553Cys
NM_001374354.1:c.4283C>G NP_001361283.1:p.Ser1428Cys
NM_005270.5:c.4709C>G NP_005261.2:p.Ser1570Cys