Canonical Allele Identifier: CA348173176
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120989188G>A , CM000664.2:g.120989188G>A GRCh38
NC_000002.11:g.121746764G>A , CM000664.1:g.121746764G>A GRCh37
NC_000002.10:g.121463234G>A NCBI36
NG_009030.1:g.196898G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361492.9:c.3223G>A MANE Select ENSP00000354586.5:p.Gly1075Ser
ENST00000452319.6:c.3274G>A ENSP00000390436.1:p.Gly1092Ser
ENST00000341310.10:c.*2322G>A ENSP00000344473.6:n.*2322G>A
ENST00000361492.8:c.3274G>A ENSP00000354586.4:p.Gly1092Ser
ENST00000438299.5:c.*2373G>A ENSP00000400593.1:n.*2373G>A
ENST00000445186.5:c.*2373G>A ENSP00000397488.1:n.*2373G>A
ENST00000452319.5:c.3274G>A ENSP00000390436.1:p.Gly1092Ser
ENST00000452692.5:c.*2322G>A ENSP00000403715.1:n.*2322G>A
NM_005270.4:c.3274G>A NP_005261.2:p.Gly1092Ser
XM_006712422.1:c.3223G>A XP_006712485.1:p.Gly1075Ser
XM_011510969.1:c.3256G>A XP_011509271.1:p.Gly1086Ser
XM_011510970.1:c.3133G>A XP_011509272.1:p.Gly1045Ser
XM_011510971.1:c.3079G>A XP_011509273.1:p.Gly1027Ser
XM_011510972.1:c.3079G>A XP_011509274.1:p.Gly1027Ser
XM_011510973.1:c.2899G>A XP_011509275.1:p.Gly967Ser
XM_011510974.1:c.2848G>A XP_011509276.1:p.Gly950Ser
XM_006712422.3:c.3223G>A XP_006712485.1:p.Gly1075Ser
XM_011510969.2:c.3526G>A XP_011509271.2:p.Gly1176Ser
XM_011510970.2:c.3133G>A XP_011509272.1:p.Gly1045Ser
XM_011510971.2:c.3079G>A XP_011509273.1:p.Gly1027Ser
XM_011510972.2:c.3175G>A XP_011509274.2:p.Gly1059Ser
XM_011510973.2:c.2899G>A XP_011509275.1:p.Gly967Ser
XM_011510974.2:c.2848G>A XP_011509276.1:p.Gly950Ser
XM_017003818.1:c.3475G>A XP_016859307.1:p.Gly1159Ser
XM_024452794.1:c.3274G>A XP_024308562.1:p.Gly1092Ser
XM_024452795.1:c.3274G>A XP_024308563.1:p.Gly1092Ser
NM_001371271.1:c.3274G>A NP_001358200.1:p.Gly1092Ser
NM_001374353.1:c.3223G>A MANE Select NP_001361282.1:p.Gly1075Ser
NM_001374354.1:c.2848G>A NP_001361283.1:p.Gly950Ser
NM_005270.5:c.3274G>A NP_005261.2:p.Gly1092Ser