Canonical Allele Identifier: CA538481543

Gene: STAT4

Linked Data

• gnomAD v2: 2-191902891-T-TCGGTGGTCGCCGTATCATTAAA
• gnomAD v3: 2-191038165-T-TCGGTGGTCGCCGTATCATTAAA
• gnomAD v4: 2-191038165-T-TCGGTGGTCGCCGTATCATTAAA
• MyVariant Identifiers: chr2:g.191902892_191902893delinsCGGTGGTCGCCGTATCATTAAAAA (hg19) ; chr2:g.191038166_191038167delinsCGGTGGTCGCCGTATCATTAAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191038165_191038166insCGGTGGTCGCCGTATCATTAAA , CM000664.2:g.191038165_191038166insCGGTGGTCGCCGTATCATTAAA	GRCh38
NC_000002.11:g.191902891_191902892insCGGTGGTCGCCGTATCATTAAA , CM000664.1:g.191902891_191902892insCGGTGGTCGCCGTATCATTAAA	GRCh37
NC_000002.10:g.191611136_191611137insCGGTGGTCGCCGTATCATTAAA	NCBI36
NG_012852.1:g.118034_118035insTTTAATGATACGGCGACCACCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG MANE Select	ENSP00000376134.2:n.1434+1033_1434+1034insTTTAATGATACGGCGACCA...
ENST00000358470.8:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG	ENSP00000351255.4:n.1434+1033_1434+1034insTTTAATGATACGGCGACCA...
ENST00000392320.6:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG	ENSP00000376134.2:n.1434+1033_1434+1034insTTTAATGATACGGCGACCA...
ENST00000470708.1:n.393+1033_393+1034insTTTAATGATACGGCGACCACCG
ENST00000495849.5:n.1502+1033_1502+1034insTTTAATGATACGGCGACCACCG
NM_001243835.1:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG	NP_001230764.1:n.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG...
NM_003151.3:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG	NP_003142.1:n.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG
XM_005246817.3:c.1461+1033_1461+1034insTTTAATGATACGGCGACCACCG	XP_005246874.1:n.1461+1033_1461+1034insTTTAATGATACGGCGACCACCG...
XM_006712719.2:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG	XP_006712782.1:n.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG...
XM_011511704.1:c.1461+1033_1461+1034insTTTAATGATACGGCGACCACCG	XP_011510006.1:n.1461+1033_1461+1034insTTTAATGATACGGCGACCACCG...
XM_011511705.1:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG	XP_011510007.1:n.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG...
XM_006712719.3:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG	XP_006712782.1:n.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG...
XM_011511705.2:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG	XP_011510007.1:n.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG...
NM_003151.4:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG MANE Select	NP_003142.1:n.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG
NM_001243835.2:c.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG	NP_001230764.1:n.1434+1033_1434+1034insTTTAATGATACGGCGACCACCG...