Canonical Allele Identifier: CA348180207
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990581T>C , CM000664.2:g.120990581T>C GRCh38
NC_000002.11:g.121748157T>C , CM000664.1:g.121748157T>C GRCh37
NC_000002.10:g.121464627T>C NCBI36
NG_009030.1:g.198291T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4616T>C MANE Select ENSP00000354586.5:p.Ile1539Thr
ENST00000452319.6:c.4667T>C ENSP00000390436.1:p.Ile1556Thr
ENST00000341310.10:c.*3715T>C ENSP00000344473.6:n.*3715T>C
ENST00000361492.8:c.4667T>C ENSP00000354586.4:p.Ile1556Thr
ENST00000438299.5:c.*2544-9T>C ENSP00000400593.1:n.*2544-9T>C
ENST00000445186.5:c.*3766T>C ENSP00000397488.1:n.*3766T>C
ENST00000452319.5:c.4667T>C ENSP00000390436.1:p.Ile1556Thr
ENST00000452692.5:c.*2493-9T>C ENSP00000403715.1:n.*2493-9T>C
NM_005270.4:c.4667T>C NP_005261.2:p.Ile1556Thr
XM_006712422.1:c.4616T>C XP_006712485.1:p.Ile1539Thr
XM_011510969.1:c.4649T>C XP_011509271.1:p.Ile1550Thr
XM_011510970.1:c.4526T>C XP_011509272.1:p.Ile1509Thr
XM_011510971.1:c.4472T>C XP_011509273.1:p.Ile1491Thr
XM_011510972.1:c.4472T>C XP_011509274.1:p.Ile1491Thr
XM_011510973.1:c.4292T>C XP_011509275.1:p.Ile1431Thr
XM_011510974.1:c.4241T>C XP_011509276.1:p.Ile1414Thr
XM_006712422.3:c.4616T>C XP_006712485.1:p.Ile1539Thr
XM_011510969.2:c.4919T>C XP_011509271.2:p.Ile1640Thr
XM_011510970.2:c.4526T>C XP_011509272.1:p.Ile1509Thr
XM_011510971.2:c.4472T>C XP_011509273.1:p.Ile1491Thr
XM_011510972.2:c.4568T>C XP_011509274.2:p.Ile1523Thr
XM_011510973.2:c.4292T>C XP_011509275.1:p.Ile1431Thr
XM_011510974.2:c.4241T>C XP_011509276.1:p.Ile1414Thr
XM_017003818.1:c.4868T>C XP_016859307.1:p.Ile1623Thr
XM_024452794.1:c.4667T>C XP_024308562.1:p.Ile1556Thr
XM_024452795.1:c.4667T>C XP_024308563.1:p.Ile1556Thr
NM_001371271.1:c.4667T>C NP_001358200.1:p.Ile1556Thr
NM_001374353.1:c.4616T>C MANE Select NP_001361282.1:p.Ile1539Thr
NM_001374354.1:c.4241T>C NP_001361283.1:p.Ile1414Thr
NM_005270.5:c.4667T>C NP_005261.2:p.Ile1556Thr