Canonical Allele Identifier: CA348161689
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120978578T>A , CM000664.2:g.120978578T>A GRCh38
NC_000002.11:g.121736154T>A , CM000664.1:g.121736154T>A GRCh37
NC_000002.10:g.121452624T>A NCBI36
NG_009030.1:g.186288T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.1462T>A MANE Select ENSP00000354586.5:p.Cys488Ser
ENST00000452319.6:c.1513T>A ENSP00000390436.1:p.Cys505Ser
ENST00000314490.15:c.526T>A ENSP00000312694.12:p.Cys176Ser
ENST00000341310.10:c.*561T>A ENSP00000344473.6:n.*561T>A
ENST00000361492.8:c.1513T>A ENSP00000354586.4:p.Cys505Ser
ENST00000435313.6:n.1487T>A
ENST00000437950.5:c.*612T>A ENSP00000415773.1:n.*612T>A
ENST00000438299.5:c.*612T>A ENSP00000400593.1:n.*612T>A
ENST00000445186.5:c.*612T>A ENSP00000397488.1:n.*612T>A
ENST00000452319.5:c.1513T>A ENSP00000390436.1:p.Cys505Ser
ENST00000452692.5:c.*561T>A ENSP00000403715.1:n.*561T>A
NM_005270.4:c.1513T>A NP_005261.2:p.Cys505Ser
XM_006712422.1:c.1462T>A XP_006712485.1:p.Cys488Ser
XM_011510969.1:c.1495T>A XP_011509271.1:p.Cys499Ser
XM_011510970.1:c.1372T>A XP_011509272.1:p.Cys458Ser
XM_011510971.1:c.1318T>A XP_011509273.1:p.Cys440Ser
XM_011510972.1:c.1318T>A XP_011509274.1:p.Cys440Ser
XM_011510973.1:c.1138T>A XP_011509275.1:p.Cys380Ser
XM_011510974.1:c.1087T>A XP_011509276.1:p.Cys363Ser
XM_006712422.3:c.1462T>A XP_006712485.1:p.Cys488Ser
XM_011510969.2:c.1765T>A XP_011509271.2:p.Cys589Ser
XM_011510970.2:c.1372T>A XP_011509272.1:p.Cys458Ser
XM_011510971.2:c.1318T>A XP_011509273.1:p.Cys440Ser
XM_011510972.2:c.1414T>A XP_011509274.2:p.Cys472Ser
XM_011510973.2:c.1138T>A XP_011509275.1:p.Cys380Ser
XM_011510974.2:c.1087T>A XP_011509276.1:p.Cys363Ser
XM_017003818.1:c.1714T>A XP_016859307.1:p.Cys572Ser
XM_024452794.1:c.1513T>A XP_024308562.1:p.Cys505Ser
XM_024452795.1:c.1513T>A XP_024308563.1:p.Cys505Ser
NM_001371271.1:c.1513T>A NP_001358200.1:p.Cys505Ser
NM_001374353.1:c.1462T>A MANE Select NP_001361282.1:p.Cys488Ser
NM_001374354.1:c.1087T>A NP_001361283.1:p.Cys363Ser
NM_005270.5:c.1513T>A NP_005261.2:p.Cys505Ser