Canonical Allele Identifier: CA2520689828

Gene: STAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191038092C>T , CM000664.2:g.191038092C>T	GRCh38
NC_000002.11:g.191902818C>T , CM000664.1:g.191902818C>T	GRCh37
NC_000002.10:g.191611063C>T	NCBI36
NG_012852.1:g.118108G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000392320.7:c.1434+1107G>A MANE Select	ENSP00000376134.2:n.1434+1107G>A
ENST00000358470.8:c.1434+1107G>A	ENSP00000351255.4:n.1434+1107G>A
ENST00000392320.6:c.1434+1107G>A	ENSP00000376134.2:n.1434+1107G>A
ENST00000470708.1:n.393+1107G>A
ENST00000495849.5:n.1502+1107G>A
NM_001243835.1:c.1434+1107G>A	NP_001230764.1:n.1434+1107G>A
NM_003151.3:c.1434+1107G>A	NP_003142.1:n.1434+1107G>A
XM_005246817.3:c.1461+1107G>A	XP_005246874.1:n.1461+1107G>A
XM_006712719.2:c.1434+1107G>A	XP_006712782.1:n.1434+1107G>A
XM_011511704.1:c.1461+1107G>A	XP_011510006.1:n.1461+1107G>A
XM_011511705.1:c.1434+1107G>A	XP_011510007.1:n.1434+1107G>A
XM_006712719.3:c.1434+1107G>A	XP_006712782.1:n.1434+1107G>A
XM_011511705.2:c.1434+1107G>A	XP_011510007.1:n.1434+1107G>A
NM_003151.4:c.1434+1107G>A MANE Select	NP_003142.1:n.1434+1107G>A
NM_001243835.2:c.1434+1107G>A	NP_001230764.1:n.1434+1107G>A