Canonical Allele Identifier: CA1316300805

Gene: STAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191038106A= , CM000664.2:g.191038106A=	GRCh38
NC_000002.11:g.191902832A= , CM000664.1:g.191902832A=	GRCh37
NC_000002.10:g.191611077A=	NCBI36
NG_012852.1:g.118094T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000392320.7:c.1434+1093T= MANE Select	ENSP00000376134.2:n.1434+1093T=
ENST00000358470.8:c.1434+1093T=	ENSP00000351255.4:n.1434+1093T=
ENST00000392320.6:c.1434+1093T=	ENSP00000376134.2:n.1434+1093T=
ENST00000470708.1:n.393+1093T=
ENST00000495849.5:n.1502+1093T=
NM_001243835.1:c.1434+1093T=	NP_001230764.1:n.1434+1093T=
NM_003151.3:c.1434+1093T=	NP_003142.1:n.1434+1093T=
XM_005246817.3:c.1461+1093T=	XP_005246874.1:n.1461+1093T=
XM_006712719.2:c.1434+1093T=	XP_006712782.1:n.1434+1093T=
XM_011511704.1:c.1461+1093T=	XP_011510006.1:n.1461+1093T=
XM_011511705.1:c.1434+1093T=	XP_011510007.1:n.1434+1093T=
XM_006712719.3:c.1434+1093T=	XP_006712782.1:n.1434+1093T=
XM_011511705.2:c.1434+1093T=	XP_011510007.1:n.1434+1093T=
NM_003151.4:c.1434+1093T= MANE Select	NP_003142.1:n.1434+1093T=
NM_001243835.2:c.1434+1093T=	NP_001230764.1:n.1434+1093T=