Canonical Allele Identifier: CA1316301268

Gene: STAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191039296G= , CM000664.2:g.191039296G=	GRCh38
NC_000002.11:g.191904022G= , CM000664.1:g.191904022G=	GRCh37
NC_000002.10:g.191612267G=	NCBI36
NG_012852.1:g.116904C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.1337C= MANE Select	ENSP00000376134.2:p.Thr446=
ENST00000358470.8:c.1337C=	ENSP00000351255.4:p.Thr446=
ENST00000392320.6:c.1337C=	ENSP00000376134.2:p.Thr446=
ENST00000470708.1:n.296C=
ENST00000495849.5:n.1405C=
NM_001243835.1:c.1337C=	NP_001230764.1:p.Thr446=
NM_003151.3:c.1337C=	NP_003142.1:p.Thr446=
XM_005246817.3:c.1364C=	XP_005246874.1:p.Thr455=
XM_006712719.2:c.1337C=	XP_006712782.1:p.Thr446=
XM_011511704.1:c.1364C=	XP_011510006.1:p.Thr455=
XM_011511705.1:c.1337C=	XP_011510007.1:p.Thr446=
XM_011511706.1:c.1364C=	XP_011510008.1:p.Thr455=
XM_006712719.3:c.1337C=	XP_006712782.1:p.Thr446=
XM_011511705.2:c.1337C=	XP_011510007.1:p.Thr446=
XM_017004784.2:c.1337C=	XP_016860273.1:p.Thr446=
NM_003151.4:c.1337C= MANE Select	NP_003142.1:p.Thr446=
NM_001243835.2:c.1337C=	NP_001230764.1:p.Thr446=