Canonical Allele Identifier: CA348180259
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990604G>C , CM000664.2:g.120990604G>C GRCh38
NC_000002.11:g.121748180G>C , CM000664.1:g.121748180G>C GRCh37
NC_000002.10:g.121464650G>C NCBI36
NG_009030.1:g.198314G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4639G>C MANE Select ENSP00000354586.5:p.Ala1547Pro
ENST00000452319.6:c.4690G>C ENSP00000390436.1:p.Ala1564Pro
ENST00000341310.10:c.*3738G>C ENSP00000344473.6:n.*3738G>C
ENST00000361492.8:c.4690G>C ENSP00000354586.4:p.Ala1564Pro
ENST00000438299.5:c.*2558G>C ENSP00000400593.1:n.*2558G>C
ENST00000445186.5:c.*3789G>C ENSP00000397488.1:n.*3789G>C
ENST00000452319.5:c.4690G>C ENSP00000390436.1:p.Ala1564Pro
ENST00000452692.5:c.*2507G>C ENSP00000403715.1:n.*2507G>C
NM_005270.4:c.4690G>C NP_005261.2:p.Ala1564Pro
XM_006712422.1:c.4639G>C XP_006712485.1:p.Ala1547Pro
XM_011510969.1:c.4672G>C XP_011509271.1:p.Ala1558Pro
XM_011510970.1:c.4549G>C XP_011509272.1:p.Ala1517Pro
XM_011510971.1:c.4495G>C XP_011509273.1:p.Ala1499Pro
XM_011510972.1:c.4495G>C XP_011509274.1:p.Ala1499Pro
XM_011510973.1:c.4315G>C XP_011509275.1:p.Ala1439Pro
XM_011510974.1:c.4264G>C XP_011509276.1:p.Ala1422Pro
XM_006712422.3:c.4639G>C XP_006712485.1:p.Ala1547Pro
XM_011510969.2:c.4942G>C XP_011509271.2:p.Ala1648Pro
XM_011510970.2:c.4549G>C XP_011509272.1:p.Ala1517Pro
XM_011510971.2:c.4495G>C XP_011509273.1:p.Ala1499Pro
XM_011510972.2:c.4591G>C XP_011509274.2:p.Ala1531Pro
XM_011510973.2:c.4315G>C XP_011509275.1:p.Ala1439Pro
XM_011510974.2:c.4264G>C XP_011509276.1:p.Ala1422Pro
XM_017003818.1:c.4891G>C XP_016859307.1:p.Ala1631Pro
XM_024452794.1:c.4690G>C XP_024308562.1:p.Ala1564Pro
XM_024452795.1:c.4690G>C XP_024308563.1:p.Ala1564Pro
NM_001371271.1:c.4690G>C NP_001358200.1:p.Ala1564Pro
NM_001374353.1:c.4639G>C MANE Select NP_001361282.1:p.Ala1547Pro
NM_001374354.1:c.4264G>C NP_001361283.1:p.Ala1422Pro
NM_005270.5:c.4690G>C NP_005261.2:p.Ala1564Pro