Canonical Allele Identifier: CA1040540449

Gene: STAT4

Linked Data

• dbSNP Id: rs1696721008
• gnomAD v3: 2-191057160-AT-A
• gnomAD v4: 2-191057160-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191057161del , CM000664.2:g.191057161del	GRCh38
NC_000002.11:g.191921887del , CM000664.1:g.191921887del	GRCh37
NC_000002.10:g.191630132del	NCBI36
NG_012852.1:g.99039del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.1206+857del MANE Select	ENSP00000376134.2:n.1206+857del
ENST00000358470.8:c.1206+857del	ENSP00000351255.4:n.1206+857del
ENST00000392320.6:c.1206+857del	ENSP00000376134.2:n.1206+857del
ENST00000495849.5:n.1274+857del
NM_001243835.1:c.1206+857del	NP_001230764.1:n.1206+857del
NM_003151.3:c.1206+857del	NP_003142.1:n.1206+857del
XM_005246817.3:c.1233+857del	XP_005246874.1:n.1233+857del
XM_006712719.2:c.1206+857del	XP_006712782.1:n.1206+857del
XM_011511704.1:c.1233+857del	XP_011510006.1:n.1233+857del
XM_011511705.1:c.1206+857del	XP_011510007.1:n.1206+857del
XM_011511706.1:c.1233+857del	XP_011510008.1:n.1233+857del
XM_006712719.3:c.1206+857del	XP_006712782.1:n.1206+857del
XM_011511705.2:c.1206+857del	XP_011510007.1:n.1206+857del
XM_017004784.2:c.1206+857del	XP_016860273.1:n.1206+857del
NM_003151.4:c.1206+857del MANE Select	NP_003142.1:n.1206+857del
NM_001243835.2:c.1206+857del	NP_001230764.1:n.1206+857del