Canonical Allele Identifier: CA1316300782

Gene: STAT4

Linked Data

• dbSNP Id: rs1696089624

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191038043_191038072del , CM000664.2:g.191038043_191038072del	GRCh38
NC_000002.11:g.191902769_191902798del , CM000664.1:g.191902769_191902798del	GRCh37
NC_000002.10:g.191611014_191611043del	NCBI36
NG_012852.1:g.118129_118158del

Transcript Alleles

HGVS	Amino-acid change
ENST00000392320.7:c.1434+1128_1434+1157del MANE Select	ENSP00000376134.2:n.1434+1128_1434+1157de...
ENST00000358470.8:c.1434+1128_1434+1157del	ENSP00000351255.4:n.1434+1128_1434+1157de...
ENST00000392320.6:c.1434+1128_1434+1157del	ENSP00000376134.2:n.1434+1128_1434+1157de...
ENST00000470708.1:n.393+1128_393+1157del
ENST00000495849.5:n.1502+1128_1502+1157del
NM_001243835.1:c.1434+1128_1434+1157del	NP_001230764.1:n.1434+1128_1434+1157del
NM_003151.3:c.1434+1128_1434+1157del	NP_003142.1:n.1434+1128_1434+1157del
XM_005246817.3:c.1461+1128_1461+1157del	XP_005246874.1:n.1461+1128_1461+1157del
XM_006712719.2:c.1434+1128_1434+1157del	XP_006712782.1:n.1434+1128_1434+1157del
XM_011511704.1:c.1461+1128_1461+1157del	XP_011510006.1:n.1461+1128_1461+1157del
XM_011511705.1:c.1434+1128_1434+1157del	XP_011510007.1:n.1434+1128_1434+1157del
XM_006712719.3:c.1434+1128_1434+1157del	XP_006712782.1:n.1434+1128_1434+1157del
XM_011511705.2:c.1434+1128_1434+1157del	XP_011510007.1:n.1434+1128_1434+1157del
NM_003151.4:c.1434+1128_1434+1157del MANE Select	NP_003142.1:n.1434+1128_1434+1157del
NM_001243835.2:c.1434+1128_1434+1157del	NP_001230764.1:n.1434+1128_1434+1157del