Canonical Allele Identifier: CA762409177

Gene: STAT4

Linked Data

• dbSNP Id: rs1224544417
• gnomAD v3: 2-191038044-CAGA-C
• gnomAD v4: 2-191038044-CAGA-C
• MyVariant Identifiers: chr2:g.191902771_191902773del (hg19) ; chr2:g.191038045_191038047del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191038047_191038049del , CM000664.2:g.191038047_191038049del	GRCh38
NC_000002.11:g.191902773_191902775del , CM000664.1:g.191902773_191902775del	GRCh37
NC_000002.10:g.191611018_191611020del	NCBI36
NG_012852.1:g.118153_118155del

Transcript Alleles

HGVS	Amino-acid change
ENST00000392320.7:c.1434+1152_1434+1154del MANE Select	ENSP00000376134.2:n.1434+1152_1434+1154de...
ENST00000358470.8:c.1434+1152_1434+1154del	ENSP00000351255.4:n.1434+1152_1434+1154de...
ENST00000392320.6:c.1434+1152_1434+1154del	ENSP00000376134.2:n.1434+1152_1434+1154de...
ENST00000470708.1:n.393+1152_393+1154del
ENST00000495849.5:n.1502+1152_1502+1154del
NM_001243835.1:c.1434+1152_1434+1154del	NP_001230764.1:n.1434+1152_1434+1154del
NM_003151.3:c.1434+1152_1434+1154del	NP_003142.1:n.1434+1152_1434+1154del
XM_005246817.3:c.1461+1152_1461+1154del	XP_005246874.1:n.1461+1152_1461+1154del
XM_006712719.2:c.1434+1152_1434+1154del	XP_006712782.1:n.1434+1152_1434+1154del
XM_011511704.1:c.1461+1152_1461+1154del	XP_011510006.1:n.1461+1152_1461+1154del
XM_011511705.1:c.1434+1152_1434+1154del	XP_011510007.1:n.1434+1152_1434+1154del
XM_006712719.3:c.1434+1152_1434+1154del	XP_006712782.1:n.1434+1152_1434+1154del
XM_011511705.2:c.1434+1152_1434+1154del	XP_011510007.1:n.1434+1152_1434+1154del
NM_003151.4:c.1434+1152_1434+1154del MANE Select	NP_003142.1:n.1434+1152_1434+1154del
NM_001243835.2:c.1434+1152_1434+1154del	NP_001230764.1:n.1434+1152_1434+1154del