Canonical Allele Identifier: CA762428734

Gene: STAT4

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191150346A>C , CM000664.2:g.191150346A>C	GRCh38
NC_000002.11:g.192015072A>C , CM000664.1:g.192015072A>C	GRCh37
NC_000002.10:g.191723317A>C	NCBI36
NG_012852.1:g.5854T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.-2+601T>G MANE Select	ENSP00000376134.2:n.-2+601T>G
ENST00000647167.1:c.-2+988T>G	ENSP00000495153.1:n.-2+988T>G
ENST00000358470.8:c.-2+988T>G	ENSP00000351255.4:n.-2+988T>G
ENST00000392320.6:c.-2+601T>G	ENSP00000376134.2:n.-2+601T>G
ENST00000409995.5:c.-2+601T>G	ENSP00000386288.1:n.-2+601T>G
ENST00000413064.5:c.-31+988T>G	ENSP00000403238.1:n.-31+988T>G
ENST00000432798.1:c.-2+601T>G	ENSP00000414322.1:n.-2+601T>G
ENST00000450994.1:c.-2+601T>G	ENSP00000412397.1:n.-2+601T>G
ENST00000495326.1:n.69+601T>G
ENST00000495849.5:n.67+601T>G
NM_001243835.1:c.-2+988T>G	NP_001230764.1:n.-2+988T>G
NM_003151.3:c.-2+601T>G	NP_003142.1:n.-2+601T>G
XM_005246817.3:c.27-2142T>G	XP_005246874.1:n.27-2142T>G
XM_006712719.2:c.-2+305T>G	XP_006712782.1:n.-2+305T>G
XM_011511704.1:c.27-2142T>G	XP_011510006.1:n.27-2142T>G
XM_011511705.1:c.-1-2142T>G	XP_011510007.1:n.-1-2142T>G
XM_011511706.1:c.27-2142T>G	XP_011510008.1:n.27-2142T>G
XM_006712719.3:c.-2+305T>G	XP_006712782.1:n.-2+305T>G
XM_011511705.2:c.-1-2142T>G	XP_011510007.1:n.-1-2142T>G
XM_017004784.2:c.-2+601T>G	XP_016860273.1:n.-2+601T>G
NM_003151.4:c.-2+601T>G MANE Select	NP_003142.1:n.-2+601T>G
NM_001243835.2:c.-2+988T>G	NP_001230764.1:n.-2+988T>G