Canonical Allele Identifier: CA1316313493

Gene: STAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191068528G= , CM000664.2:g.191068528G=	GRCh38
NC_000002.11:g.191933254G= , CM000664.1:g.191933254G=	GRCh37
NC_000002.10:g.191641499G=	NCBI36
NG_012852.1:g.87672C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.544+1165C= MANE Select	ENSP00000376134.2:n.544+1165C=
ENST00000647167.1:c.*35C=	ENSP00000495153.1:n.*35C=
ENST00000358470.8:c.544+1165C=	ENSP00000351255.4:n.544+1165C=
ENST00000392320.6:c.544+1165C=	ENSP00000376134.2:n.544+1165C=
ENST00000495849.5:n.612+1165C=
NM_001243835.1:c.544+1165C=	NP_001230764.1:n.544+1165C=
NM_003151.3:c.544+1165C=	NP_003142.1:n.544+1165C=
XM_005246817.3:c.571+1165C=	XP_005246874.1:n.571+1165C=
XM_006712719.2:c.544+1165C=	XP_006712782.1:n.544+1165C=
XM_011511704.1:c.571+1165C=	XP_011510006.1:n.571+1165C=
XM_011511705.1:c.544+1165C=	XP_011510007.1:n.544+1165C=
XM_011511706.1:c.571+1165C=	XP_011510008.1:n.571+1165C=
XM_006712719.3:c.544+1165C=	XP_006712782.1:n.544+1165C=
XM_011511705.2:c.544+1165C=	XP_011510007.1:n.544+1165C=
XM_017004784.2:c.544+1165C=	XP_016860273.1:n.544+1165C=
NM_003151.4:c.544+1165C= MANE Select	NP_003142.1:n.544+1165C=
NM_001243835.2:c.544+1165C=	NP_001230764.1:n.544+1165C=