Canonical Allele Identifier: CA348161491
Gene: GLI2 HGNC NCBI

Linked Data

dbSNP Id: rs2105050724

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120978488C>T , CM000664.2:g.120978488C>T GRCh38
NC_000002.11:g.121736064C>T , CM000664.1:g.121736064C>T GRCh37
NC_000002.10:g.121452534C>T NCBI36
NG_009030.1:g.186198C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.1372C>T MANE Select ENSP00000354586.5:p.Gln458Ter
ENST00000452319.6:c.1423C>T ENSP00000390436.1:p.Gln475Ter
ENST00000314490.15:c.436C>T ENSP00000312694.12:p.Gln146Ter
ENST00000341310.10:c.*471C>T ENSP00000344473.6:n.*471C>T
ENST00000361492.8:c.1423C>T ENSP00000354586.4:p.Gln475Ter
ENST00000435313.6:n.1397C>T
ENST00000437950.5:c.*522C>T ENSP00000415773.1:n.*522C>T
ENST00000438299.5:c.*522C>T ENSP00000400593.1:n.*522C>T
ENST00000445186.5:c.*522C>T ENSP00000397488.1:n.*522C>T
ENST00000452319.5:c.1423C>T ENSP00000390436.1:p.Gln475Ter
ENST00000452692.5:c.*471C>T ENSP00000403715.1:n.*471C>T
NM_005270.4:c.1423C>T NP_005261.2:p.Gln475Ter
XM_006712422.1:c.1372C>T XP_006712485.1:p.Gln458Ter
XM_011510969.1:c.1405C>T XP_011509271.1:p.Gln469Ter
XM_011510970.1:c.1282C>T XP_011509272.1:p.Gln428Ter
XM_011510971.1:c.1228C>T XP_011509273.1:p.Gln410Ter
XM_011510972.1:c.1228C>T XP_011509274.1:p.Gln410Ter
XM_011510973.1:c.1048C>T XP_011509275.1:p.Gln350Ter
XM_011510974.1:c.997C>T XP_011509276.1:p.Gln333Ter
XM_006712422.3:c.1372C>T XP_006712485.1:p.Gln458Ter
XM_011510969.2:c.1675C>T XP_011509271.2:p.Gln559Ter
XM_011510970.2:c.1282C>T XP_011509272.1:p.Gln428Ter
XM_011510971.2:c.1228C>T XP_011509273.1:p.Gln410Ter
XM_011510972.2:c.1324C>T XP_011509274.2:p.Gln442Ter
XM_011510973.2:c.1048C>T XP_011509275.1:p.Gln350Ter
XM_011510974.2:c.997C>T XP_011509276.1:p.Gln333Ter
XM_017003818.1:c.1624C>T XP_016859307.1:p.Gln542Ter
XM_024452794.1:c.1423C>T XP_024308562.1:p.Gln475Ter
XM_024452795.1:c.1423C>T XP_024308563.1:p.Gln475Ter
NM_001371271.1:c.1423C>T NP_001358200.1:p.Gln475Ter
NM_001374353.1:c.1372C>T MANE Select NP_001361282.1:p.Gln458Ter
NM_001374354.1:c.997C>T NP_001361283.1:p.Gln333Ter
NM_005270.5:c.1423C>T NP_005261.2:p.Gln475Ter