Canonical Allele Identifier: CA11205791

Gene: STAT4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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