Canonical Allele Identifier: CA62687974

Gene: STAT4

Linked Data

• dbSNP Id: rs750644772
• MyVariant Identifiers: chr2:g.191921893_191921894insG (hg19) ; chr2:g.191057167_191057168insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191057168dup , CM000664.2:g.191057168dup	GRCh38
NC_000002.11:g.191921894dup , CM000664.1:g.191921894dup	GRCh37
NC_000002.10:g.191630139dup	NCBI36
NG_012852.1:g.99032dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.1206+850dup MANE Select	ENSP00000376134.2:n.1206+850dup
ENST00000358470.8:c.1206+850dup	ENSP00000351255.4:n.1206+850dup
ENST00000392320.6:c.1206+850dup	ENSP00000376134.2:n.1206+850dup
ENST00000495849.5:n.1274+850dup
NM_001243835.1:c.1206+850dup	NP_001230764.1:n.1206+850dup
NM_003151.3:c.1206+850dup	NP_003142.1:n.1206+850dup
XM_005246817.3:c.1233+850dup	XP_005246874.1:n.1233+850dup
XM_006712719.2:c.1206+850dup	XP_006712782.1:n.1206+850dup
XM_011511704.1:c.1233+850dup	XP_011510006.1:n.1233+850dup
XM_011511705.1:c.1206+850dup	XP_011510007.1:n.1206+850dup
XM_011511706.1:c.1233+850dup	XP_011510008.1:n.1233+850dup
XM_006712719.3:c.1206+850dup	XP_006712782.1:n.1206+850dup
XM_011511705.2:c.1206+850dup	XP_011510007.1:n.1206+850dup
XM_017004784.2:c.1206+850dup	XP_016860273.1:n.1206+850dup
NM_003151.4:c.1206+850dup MANE Select	NP_003142.1:n.1206+850dup
NM_001243835.2:c.1206+850dup	NP_001230764.1:n.1206+850dup