Canonical Allele Identifier: CA348180108
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990527C>T , CM000664.2:g.120990527C>T GRCh38
NC_000002.11:g.121748103C>T , CM000664.1:g.121748103C>T GRCh37
NC_000002.10:g.121464573C>T NCBI36
NG_009030.1:g.198237C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4562C>T MANE Select ENSP00000354586.5:p.Ser1521Phe
ENST00000452319.6:c.4613C>T ENSP00000390436.1:p.Ser1538Phe
ENST00000341310.10:c.*3661C>T ENSP00000344473.6:n.*3661C>T
ENST00000361492.8:c.4613C>T ENSP00000354586.4:p.Ser1538Phe
ENST00000438299.5:c.*2544-63C>T ENSP00000400593.1:n.*2544-63C>T
ENST00000445186.5:c.*3712C>T ENSP00000397488.1:n.*3712C>T
ENST00000452319.5:c.4613C>T ENSP00000390436.1:p.Ser1538Phe
ENST00000452692.5:c.*2493-63C>T ENSP00000403715.1:n.*2493-63C>T
NM_005270.4:c.4613C>T NP_005261.2:p.Ser1538Phe
XM_006712422.1:c.4562C>T XP_006712485.1:p.Ser1521Phe
XM_011510969.1:c.4595C>T XP_011509271.1:p.Ser1532Phe
XM_011510970.1:c.4472C>T XP_011509272.1:p.Ser1491Phe
XM_011510971.1:c.4418C>T XP_011509273.1:p.Ser1473Phe
XM_011510972.1:c.4418C>T XP_011509274.1:p.Ser1473Phe
XM_011510973.1:c.4238C>T XP_011509275.1:p.Ser1413Phe
XM_011510974.1:c.4187C>T XP_011509276.1:p.Ser1396Phe
XM_006712422.3:c.4562C>T XP_006712485.1:p.Ser1521Phe
XM_011510969.2:c.4865C>T XP_011509271.2:p.Ser1622Phe
XM_011510970.2:c.4472C>T XP_011509272.1:p.Ser1491Phe
XM_011510971.2:c.4418C>T XP_011509273.1:p.Ser1473Phe
XM_011510972.2:c.4514C>T XP_011509274.2:p.Ser1505Phe
XM_011510973.2:c.4238C>T XP_011509275.1:p.Ser1413Phe
XM_011510974.2:c.4187C>T XP_011509276.1:p.Ser1396Phe
XM_017003818.1:c.4814C>T XP_016859307.1:p.Ser1605Phe
XM_024452794.1:c.4613C>T XP_024308562.1:p.Ser1538Phe
XM_024452795.1:c.4613C>T XP_024308563.1:p.Ser1538Phe
NM_001371271.1:c.4613C>T NP_001358200.1:p.Ser1538Phe
NM_001374353.1:c.4562C>T MANE Select NP_001361282.1:p.Ser1521Phe
NM_001374354.1:c.4187C>T NP_001361283.1:p.Ser1396Phe
NM_005270.5:c.4613C>T NP_005261.2:p.Ser1538Phe