Canonical Allele Identifier: CA62687948

Gene: STAT4

Linked Data

• dbSNP Id: rs1053429125
• gnomAD v3: 2-191057115-CT-C
• gnomAD v4: 2-191057115-CT-C
• MyVariant Identifiers: chr2:g.191921842del (hg19) ; chr2:g.191057116del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191057119del , CM000664.2:g.191057119del	GRCh38
NC_000002.11:g.191921845del , CM000664.1:g.191921845del	GRCh37
NC_000002.10:g.191630090del	NCBI36
NG_012852.1:g.99084del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.1206+902del MANE Select	ENSP00000376134.2:n.1206+902del
ENST00000358470.8:c.1206+902del	ENSP00000351255.4:n.1206+902del
ENST00000392320.6:c.1206+902del	ENSP00000376134.2:n.1206+902del
ENST00000495849.5:n.1274+902del
NM_001243835.1:c.1206+902del	NP_001230764.1:n.1206+902del
NM_003151.3:c.1206+902del	NP_003142.1:n.1206+902del
XM_005246817.3:c.1233+902del	XP_005246874.1:n.1233+902del
XM_006712719.2:c.1206+902del	XP_006712782.1:n.1206+902del
XM_011511704.1:c.1233+902del	XP_011510006.1:n.1233+902del
XM_011511705.1:c.1206+902del	XP_011510007.1:n.1206+902del
XM_011511706.1:c.1233+902del	XP_011510008.1:n.1233+902del
XM_006712719.3:c.1206+902del	XP_006712782.1:n.1206+902del
XM_011511705.2:c.1206+902del	XP_011510007.1:n.1206+902del
XM_017004784.2:c.1206+902del	XP_016860273.1:n.1206+902del
NM_003151.4:c.1206+902del MANE Select	NP_003142.1:n.1206+902del
NM_001243835.2:c.1206+902del	NP_001230764.1:n.1206+902del