Canonical Allele Identifier: CA348180246
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990599A>T , CM000664.2:g.120990599A>T GRCh38
NC_000002.11:g.121748175A>T , CM000664.1:g.121748175A>T GRCh37
NC_000002.10:g.121464645A>T NCBI36
NG_009030.1:g.198309A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4634A>T MANE Select ENSP00000354586.5:p.Asn1545Ile
ENST00000452319.6:c.4685A>T ENSP00000390436.1:p.Asn1562Ile
ENST00000341310.10:c.*3733A>T ENSP00000344473.6:n.*3733A>T
ENST00000361492.8:c.4685A>T ENSP00000354586.4:p.Asn1562Ile
ENST00000438299.5:c.*2553A>T ENSP00000400593.1:n.*2553A>T
ENST00000445186.5:c.*3784A>T ENSP00000397488.1:n.*3784A>T
ENST00000452319.5:c.4685A>T ENSP00000390436.1:p.Asn1562Ile
ENST00000452692.5:c.*2502A>T ENSP00000403715.1:n.*2502A>T
NM_005270.4:c.4685A>T NP_005261.2:p.Asn1562Ile
XM_006712422.1:c.4634A>T XP_006712485.1:p.Asn1545Ile
XM_011510969.1:c.4667A>T XP_011509271.1:p.Asn1556Ile
XM_011510970.1:c.4544A>T XP_011509272.1:p.Asn1515Ile
XM_011510971.1:c.4490A>T XP_011509273.1:p.Asn1497Ile
XM_011510972.1:c.4490A>T XP_011509274.1:p.Asn1497Ile
XM_011510973.1:c.4310A>T XP_011509275.1:p.Asn1437Ile
XM_011510974.1:c.4259A>T XP_011509276.1:p.Asn1420Ile
XM_006712422.3:c.4634A>T XP_006712485.1:p.Asn1545Ile
XM_011510969.2:c.4937A>T XP_011509271.2:p.Asn1646Ile
XM_011510970.2:c.4544A>T XP_011509272.1:p.Asn1515Ile
XM_011510971.2:c.4490A>T XP_011509273.1:p.Asn1497Ile
XM_011510972.2:c.4586A>T XP_011509274.2:p.Asn1529Ile
XM_011510973.2:c.4310A>T XP_011509275.1:p.Asn1437Ile
XM_011510974.2:c.4259A>T XP_011509276.1:p.Asn1420Ile
XM_017003818.1:c.4886A>T XP_016859307.1:p.Asn1629Ile
XM_024452794.1:c.4685A>T XP_024308562.1:p.Asn1562Ile
XM_024452795.1:c.4685A>T XP_024308563.1:p.Asn1562Ile
NM_001371271.1:c.4685A>T NP_001358200.1:p.Asn1562Ile
NM_001374353.1:c.4634A>T MANE Select NP_001361282.1:p.Asn1545Ile
NM_001374354.1:c.4259A>T NP_001361283.1:p.Asn1420Ile
NM_005270.5:c.4685A>T NP_005261.2:p.Asn1562Ile