Canonical Allele Identifier: CA348180495
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990664A>C , CM000664.2:g.120990664A>C GRCh38
NC_000002.11:g.121748240A>C , CM000664.1:g.121748240A>C GRCh37
NC_000002.10:g.121464710A>C NCBI36
NG_009030.1:g.198374A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4699A>C MANE Select ENSP00000354586.5:p.Met1567Leu
ENST00000452319.6:c.4750A>C ENSP00000390436.1:p.Met1584Leu
ENST00000341310.10:c.*3798A>C ENSP00000344473.6:n.*3798A>C
ENST00000361492.8:c.4750A>C ENSP00000354586.4:p.Met1584Leu
ENST00000438299.5:c.*2618A>C ENSP00000400593.1:n.*2618A>C
ENST00000445186.5:c.*3849A>C ENSP00000397488.1:n.*3849A>C
ENST00000452319.5:c.4750A>C ENSP00000390436.1:p.Met1584Leu
ENST00000452692.5:c.*2567A>C ENSP00000403715.1:n.*2567A>C
NM_005270.4:c.4750A>C NP_005261.2:p.Met1584Leu
XM_006712422.1:c.4699A>C XP_006712485.1:p.Met1567Leu
XM_011510969.1:c.4732A>C XP_011509271.1:p.Met1578Leu
XM_011510970.1:c.4609A>C XP_011509272.1:p.Met1537Leu
XM_011510971.1:c.4555A>C XP_011509273.1:p.Met1519Leu
XM_011510972.1:c.4555A>C XP_011509274.1:p.Met1519Leu
XM_011510973.1:c.4375A>C XP_011509275.1:p.Met1459Leu
XM_011510974.1:c.4324A>C XP_011509276.1:p.Met1442Leu
XM_006712422.3:c.4699A>C XP_006712485.1:p.Met1567Leu
XM_011510969.2:c.5002A>C XP_011509271.2:p.Met1668Leu
XM_011510970.2:c.4609A>C XP_011509272.1:p.Met1537Leu
XM_011510971.2:c.4555A>C XP_011509273.1:p.Met1519Leu
XM_011510972.2:c.4651A>C XP_011509274.2:p.Met1551Leu
XM_011510973.2:c.4375A>C XP_011509275.1:p.Met1459Leu
XM_011510974.2:c.4324A>C XP_011509276.1:p.Met1442Leu
XM_017003818.1:c.4951A>C XP_016859307.1:p.Met1651Leu
XM_024452794.1:c.4750A>C XP_024308562.1:p.Met1584Leu
XM_024452795.1:c.4750A>C XP_024308563.1:p.Met1584Leu
NM_001371271.1:c.4750A>C NP_001358200.1:p.Met1584Leu
NM_001374353.1:c.4699A>C MANE Select NP_001361282.1:p.Met1567Leu
NM_001374354.1:c.4324A>C NP_001361283.1:p.Met1442Leu
NM_005270.5:c.4750A>C NP_005261.2:p.Met1584Leu