Canonical Allele Identifier: CA762406525

Gene: STAT4

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191075725G>T , CM000664.2:g.191075725G>T	GRCh38
NC_000002.11:g.191940451G>T , CM000664.1:g.191940451G>T	GRCh37
NC_000002.10:g.191648696G>T	NCBI36
NG_012852.1:g.80475C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.372+502C>A MANE Select	ENSP00000376134.2:n.372+502C>A
ENST00000647167.1:c.372+502C>A	ENSP00000495153.1:n.372+502C>A
ENST00000358470.8:c.372+502C>A	ENSP00000351255.4:n.372+502C>A
ENST00000392320.6:c.372+502C>A	ENSP00000376134.2:n.372+502C>A
ENST00000495849.5:n.440+502C>A
NM_001243835.1:c.372+502C>A	NP_001230764.1:n.372+502C>A
NM_003151.3:c.372+502C>A	NP_003142.1:n.372+502C>A
XM_005246817.3:c.399+502C>A	XP_005246874.1:n.399+502C>A
XM_006712719.2:c.372+502C>A	XP_006712782.1:n.372+502C>A
XM_011511704.1:c.399+502C>A	XP_011510006.1:n.399+502C>A
XM_011511705.1:c.372+502C>A	XP_011510007.1:n.372+502C>A
XM_011511706.1:c.399+502C>A	XP_011510008.1:n.399+502C>A
XM_006712719.3:c.372+502C>A	XP_006712782.1:n.372+502C>A
XM_011511705.2:c.372+502C>A	XP_011510007.1:n.372+502C>A
XM_017004784.2:c.372+502C>A	XP_016860273.1:n.372+502C>A
NM_003151.4:c.372+502C>A MANE Select	NP_003142.1:n.372+502C>A
NM_001243835.2:c.372+502C>A	NP_001230764.1:n.372+502C>A