Canonical Allele Identifier: CA762420143
Gene: STAT4 HGNC NCBI

Linked Data

dbSNP Id: rs1339853012

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191105503_191105505del , CM000664.2:g.191105503_191105505del GRCh38
NC_000002.11:g.191970229_191970231del , CM000664.1:g.191970229_191970231del GRCh37
NC_000002.10:g.191678474_191678476del NCBI36
NG_012852.1:g.50699_50701del

Transcript Alleles

HGVS Amino-acid Change
ENST00000392320.7:c.274-29176_274-29174del MANE Select ENSP00000376134.2:n.274-29176_274-29174del
ENST00000647167.1:c.274-29176_274-29174del ENSP00000495153.1:n.274-29176_274-29174del
ENST00000358470.8:c.274-29176_274-29174del ENSP00000351255.4:n.274-29176_274-29174del
ENST00000392320.6:c.274-29176_274-29174del ENSP00000376134.2:n.274-29176_274-29174del
ENST00000413064.5:c.193-29176_193-29174del ENSP00000403238.1:n.193-29176_193-29174del
ENST00000495326.1:n.344-29176_344-29174del
ENST00000495849.5:n.342-29176_342-29174del
NM_001243835.1:c.274-29176_274-29174del NP_001230764.1:n.274-29176_274-29174del
NM_003151.3:c.274-29176_274-29174del NP_003142.1:n.274-29176_274-29174del
XM_005246817.3:c.301-29176_301-29174del XP_005246874.1:n.301-29176_301-29174del
XM_006712719.2:c.274-29176_274-29174del XP_006712782.1:n.274-29176_274-29174del
XM_011511704.1:c.301-29176_301-29174del XP_011510006.1:n.301-29176_301-29174del
XM_011511705.1:c.274-29176_274-29174del XP_011510007.1:n.274-29176_274-29174del
XM_011511706.1:c.301-29176_301-29174del XP_011510008.1:n.301-29176_301-29174del
XM_006712719.3:c.274-29176_274-29174del XP_006712782.1:n.274-29176_274-29174del
XM_011511705.2:c.274-29176_274-29174del XP_011510007.1:n.274-29176_274-29174del
XM_017004784.2:c.274-29176_274-29174del XP_016860273.1:n.274-29176_274-29174del
NM_003151.4:c.274-29176_274-29174del MANE Select NP_003142.1:n.274-29176_274-29174del
NM_001243835.2:c.274-29176_274-29174del NP_001230764.1:n.274-29176_274-29174del