Canonical Allele Identifier: CA11306335
Gene: STAT4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191040163C>T , CM000664.2:g.191040163C>T GRCh38
NC_000002.11:g.191904889C>T , CM000664.1:g.191904889C>T GRCh37
NC_000002.10:g.191613134C>T NCBI36
NG_012852.1:g.116037G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392320.7:c.1336-866G>A MANE Select ENSP00000376134.2:n.1336-866G>A
ENST00000358470.8:c.1336-866G>A ENSP00000351255.4:n.1336-866G>A
ENST00000392320.6:c.1336-866G>A ENSP00000376134.2:n.1336-866G>A
ENST00000470708.1:n.295-866G>A
ENST00000495849.5:n.1404-866G>A
NM_001243835.1:c.1336-866G>A NP_001230764.1:n.1336-866G>A
NM_003151.3:c.1336-866G>A NP_003142.1:n.1336-866G>A
XM_005246817.3:c.1363-866G>A XP_005246874.1:n.1363-866G>A
XM_006712719.2:c.1336-866G>A XP_006712782.1:n.1336-866G>A
XM_011511704.1:c.1363-866G>A XP_011510006.1:n.1363-866G>A
XM_011511705.1:c.1336-866G>A XP_011510007.1:n.1336-866G>A
XM_011511706.1:c.1363-866G>A XP_011510008.1:n.1363-866G>A
XM_006712719.3:c.1336-866G>A XP_006712782.1:n.1336-866G>A
XM_011511705.2:c.1336-866G>A XP_011510007.1:n.1336-866G>A
XM_017004784.2:c.1336-866G>A XP_016860273.1:n.1336-866G>A
NM_003151.4:c.1336-866G>A MANE Select NP_003142.1:n.1336-866G>A
NM_001243835.2:c.1336-866G>A NP_001230764.1:n.1336-866G>A
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