Canonical Allele Identifier: CA348161476
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120978481C>A , CM000664.2:g.120978481C>A GRCh38
NC_000002.11:g.121736057C>A , CM000664.1:g.121736057C>A GRCh37
NC_000002.10:g.121452527C>A NCBI36
NG_009030.1:g.186191C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.1365C>A MANE Select ENSP00000354586.5:p.Cys455Ter
ENST00000452319.6:c.1416C>A ENSP00000390436.1:p.Cys472Ter
ENST00000314490.15:c.429C>A ENSP00000312694.12:p.Cys143Ter
ENST00000341310.10:c.*464C>A ENSP00000344473.6:n.*464C>A
ENST00000361492.8:c.1416C>A ENSP00000354586.4:p.Cys472Ter
ENST00000435313.6:n.1390C>A
ENST00000437950.5:c.*515C>A ENSP00000415773.1:n.*515C>A
ENST00000438299.5:c.*515C>A ENSP00000400593.1:n.*515C>A
ENST00000445186.5:c.*515C>A ENSP00000397488.1:n.*515C>A
ENST00000452319.5:c.1416C>A ENSP00000390436.1:p.Cys472Ter
ENST00000452692.5:c.*464C>A ENSP00000403715.1:n.*464C>A
NM_005270.4:c.1416C>A NP_005261.2:p.Cys472Ter
XM_006712422.1:c.1365C>A XP_006712485.1:p.Cys455Ter
XM_011510969.1:c.1398C>A XP_011509271.1:p.Cys466Ter
XM_011510970.1:c.1275C>A XP_011509272.1:p.Cys425Ter
XM_011510971.1:c.1221C>A XP_011509273.1:p.Cys407Ter
XM_011510972.1:c.1221C>A XP_011509274.1:p.Cys407Ter
XM_011510973.1:c.1041C>A XP_011509275.1:p.Cys347Ter
XM_011510974.1:c.990C>A XP_011509276.1:p.Cys330Ter
XM_006712422.3:c.1365C>A XP_006712485.1:p.Cys455Ter
XM_011510969.2:c.1668C>A XP_011509271.2:p.Cys556Ter
XM_011510970.2:c.1275C>A XP_011509272.1:p.Cys425Ter
XM_011510971.2:c.1221C>A XP_011509273.1:p.Cys407Ter
XM_011510972.2:c.1317C>A XP_011509274.2:p.Cys439Ter
XM_011510973.2:c.1041C>A XP_011509275.1:p.Cys347Ter
XM_011510974.2:c.990C>A XP_011509276.1:p.Cys330Ter
XM_017003818.1:c.1617C>A XP_016859307.1:p.Cys539Ter
XM_024452794.1:c.1416C>A XP_024308562.1:p.Cys472Ter
XM_024452795.1:c.1416C>A XP_024308563.1:p.Cys472Ter
NM_001371271.1:c.1416C>A NP_001358200.1:p.Cys472Ter
NM_001374353.1:c.1365C>A MANE Select NP_001361282.1:p.Cys455Ter
NM_001374354.1:c.990C>A NP_001361283.1:p.Cys330Ter
NM_005270.5:c.1416C>A NP_005261.2:p.Cys472Ter