Canonical Allele Identifier: CA62982331

Gene: STAT4

Linked Data

• dbSNP Id: rs35019054
• MyVariant Identifiers: chr2:g.191970220_191970221insC (hg19) ; chr2:g.191105494_191105495insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191105494_191105495insC , CM000664.2:g.191105494_191105495insC	GRCh38
NC_000002.11:g.191970220_191970221insC , CM000664.1:g.191970220_191970221insC	GRCh37
NC_000002.10:g.191678465_191678466insC	NCBI36
NG_012852.1:g.50705_50706insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.274-29170_274-29169insG MANE Select	ENSP00000376134.2:n.274-29170_274-29169insG
ENST00000647167.1:c.274-29170_274-29169insG	ENSP00000495153.1:n.274-29170_274-29169insG
ENST00000358470.8:c.274-29170_274-29169insG	ENSP00000351255.4:n.274-29170_274-29169insG
ENST00000392320.6:c.274-29170_274-29169insG	ENSP00000376134.2:n.274-29170_274-29169insG
ENST00000413064.5:c.193-29170_193-29169insG	ENSP00000403238.1:n.193-29170_193-29169insG
ENST00000495326.1:n.344-29170_344-29169insG
ENST00000495849.5:n.342-29170_342-29169insG
NM_001243835.1:c.274-29170_274-29169insG	NP_001230764.1:n.274-29170_274-29169insG
NM_003151.3:c.274-29170_274-29169insG	NP_003142.1:n.274-29170_274-29169insG
XM_005246817.3:c.301-29170_301-29169insG	XP_005246874.1:n.301-29170_301-29169insG
XM_006712719.2:c.274-29170_274-29169insG	XP_006712782.1:n.274-29170_274-29169insG
XM_011511704.1:c.301-29170_301-29169insG	XP_011510006.1:n.301-29170_301-29169insG
XM_011511705.1:c.274-29170_274-29169insG	XP_011510007.1:n.274-29170_274-29169insG
XM_011511706.1:c.301-29170_301-29169insG	XP_011510008.1:n.301-29170_301-29169insG
XM_006712719.3:c.274-29170_274-29169insG	XP_006712782.1:n.274-29170_274-29169insG
XM_011511705.2:c.274-29170_274-29169insG	XP_011510007.1:n.274-29170_274-29169insG
XM_017004784.2:c.274-29170_274-29169insG	XP_016860273.1:n.274-29170_274-29169insG
NM_003151.4:c.274-29170_274-29169insG MANE Select	NP_003142.1:n.274-29170_274-29169insG
NM_001243835.2:c.274-29170_274-29169insG	NP_001230764.1:n.274-29170_274-29169insG