Canonical Allele Identifier: CA348161385
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120978443A>G , CM000664.2:g.120978443A>G GRCh38
NC_000002.11:g.121736019A>G , CM000664.1:g.121736019A>G GRCh37
NC_000002.10:g.121452489A>G NCBI36
NG_009030.1:g.186153A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.1327A>G MANE Select ENSP00000354586.5:p.Asn443Asp
ENST00000452319.6:c.1378A>G ENSP00000390436.1:p.Asn460Asp
ENST00000314490.15:c.391A>G ENSP00000312694.12:p.Asn131Asp
ENST00000341310.10:c.*426A>G ENSP00000344473.6:n.*426A>G
ENST00000361492.8:c.1378A>G ENSP00000354586.4:p.Asn460Asp
ENST00000435313.6:n.1352A>G
ENST00000437950.5:c.*477A>G ENSP00000415773.1:n.*477A>G
ENST00000438299.5:c.*477A>G ENSP00000400593.1:n.*477A>G
ENST00000445186.5:c.*477A>G ENSP00000397488.1:n.*477A>G
ENST00000452319.5:c.1378A>G ENSP00000390436.1:p.Asn460Asp
ENST00000452692.5:c.*426A>G ENSP00000403715.1:n.*426A>G
NM_005270.4:c.1378A>G NP_005261.2:p.Asn460Asp
XM_006712422.1:c.1327A>G XP_006712485.1:p.Asn443Asp
XM_011510969.1:c.1360A>G XP_011509271.1:p.Asn454Asp
XM_011510970.1:c.1237A>G XP_011509272.1:p.Asn413Asp
XM_011510971.1:c.1183A>G XP_011509273.1:p.Asn395Asp
XM_011510972.1:c.1183A>G XP_011509274.1:p.Asn395Asp
XM_011510973.1:c.1003A>G XP_011509275.1:p.Asn335Asp
XM_011510974.1:c.952A>G XP_011509276.1:p.Asn318Asp
XM_006712422.3:c.1327A>G XP_006712485.1:p.Asn443Asp
XM_011510969.2:c.1630A>G XP_011509271.2:p.Asn544Asp
XM_011510970.2:c.1237A>G XP_011509272.1:p.Asn413Asp
XM_011510971.2:c.1183A>G XP_011509273.1:p.Asn395Asp
XM_011510972.2:c.1279A>G XP_011509274.2:p.Asn427Asp
XM_011510973.2:c.1003A>G XP_011509275.1:p.Asn335Asp
XM_011510974.2:c.952A>G XP_011509276.1:p.Asn318Asp
XM_017003818.1:c.1579A>G XP_016859307.1:p.Asn527Asp
XM_024452794.1:c.1378A>G XP_024308562.1:p.Asn460Asp
XM_024452795.1:c.1378A>G XP_024308563.1:p.Asn460Asp
NM_001371271.1:c.1378A>G NP_001358200.1:p.Asn460Asp
NM_001374353.1:c.1327A>G MANE Select NP_001361282.1:p.Asn443Asp
NM_001374354.1:c.952A>G NP_001361283.1:p.Asn318Asp
NM_005270.5:c.1378A>G NP_005261.2:p.Asn460Asp