Canonical Allele Identifier: CA348180267
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990608T>C , CM000664.2:g.120990608T>C GRCh38
NC_000002.11:g.121748184T>C , CM000664.1:g.121748184T>C GRCh37
NC_000002.10:g.121464654T>C NCBI36
NG_009030.1:g.198318T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4643T>C MANE Select ENSP00000354586.5:p.Val1548Ala
ENST00000452319.6:c.4694T>C ENSP00000390436.1:p.Val1565Ala
ENST00000341310.10:c.*3742T>C ENSP00000344473.6:n.*3742T>C
ENST00000361492.8:c.4694T>C ENSP00000354586.4:p.Val1565Ala
ENST00000438299.5:c.*2562T>C ENSP00000400593.1:n.*2562T>C
ENST00000445186.5:c.*3793T>C ENSP00000397488.1:n.*3793T>C
ENST00000452319.5:c.4694T>C ENSP00000390436.1:p.Val1565Ala
ENST00000452692.5:c.*2511T>C ENSP00000403715.1:n.*2511T>C
NM_005270.4:c.4694T>C NP_005261.2:p.Val1565Ala
XM_006712422.1:c.4643T>C XP_006712485.1:p.Val1548Ala
XM_011510969.1:c.4676T>C XP_011509271.1:p.Val1559Ala
XM_011510970.1:c.4553T>C XP_011509272.1:p.Val1518Ala
XM_011510971.1:c.4499T>C XP_011509273.1:p.Val1500Ala
XM_011510972.1:c.4499T>C XP_011509274.1:p.Val1500Ala
XM_011510973.1:c.4319T>C XP_011509275.1:p.Val1440Ala
XM_011510974.1:c.4268T>C XP_011509276.1:p.Val1423Ala
XM_006712422.3:c.4643T>C XP_006712485.1:p.Val1548Ala
XM_011510969.2:c.4946T>C XP_011509271.2:p.Val1649Ala
XM_011510970.2:c.4553T>C XP_011509272.1:p.Val1518Ala
XM_011510971.2:c.4499T>C XP_011509273.1:p.Val1500Ala
XM_011510972.2:c.4595T>C XP_011509274.2:p.Val1532Ala
XM_011510973.2:c.4319T>C XP_011509275.1:p.Val1440Ala
XM_011510974.2:c.4268T>C XP_011509276.1:p.Val1423Ala
XM_017003818.1:c.4895T>C XP_016859307.1:p.Val1632Ala
XM_024452794.1:c.4694T>C XP_024308562.1:p.Val1565Ala
XM_024452795.1:c.4694T>C XP_024308563.1:p.Val1565Ala
NM_001371271.1:c.4694T>C NP_001358200.1:p.Val1565Ala
NM_001374353.1:c.4643T>C MANE Select NP_001361282.1:p.Val1548Ala
NM_001374354.1:c.4268T>C NP_001361283.1:p.Val1423Ala
NM_005270.5:c.4694T>C NP_005261.2:p.Val1565Ala