Canonical Allele Identifier: CA11237137

Gene: STAT4

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191032814C>T , CM000664.2:g.191032814C>T	GRCh38
NC_000002.11:g.191897540C>T , CM000664.1:g.191897540C>T	GRCh37
NC_000002.10:g.191605785C>T	NCBI36
NG_012852.1:g.123386G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.2044+144G>A MANE Select	ENSP00000376134.2:n.2044+144G>A
ENST00000358470.8:c.2044+144G>A	ENSP00000351255.4:n.2044+144G>A
ENST00000392320.6:c.2044+144G>A	ENSP00000376134.2:n.2044+144G>A
ENST00000463951.1:n.310+144G>A
NM_001243835.1:c.2044+144G>A	NP_001230764.1:n.2044+144G>A
NM_003151.3:c.2044+144G>A	NP_003142.1:n.2044+144G>A
XM_005246817.3:c.2071+144G>A	XP_005246874.1:n.2071+144G>A
XM_006712719.2:c.2044+144G>A	XP_006712782.1:n.2044+144G>A
XM_011511704.1:c.2071+144G>A	XP_011510006.1:n.2071+144G>A
XM_011511705.1:c.2044+144G>A	XP_011510007.1:n.2044+144G>A
XM_006712719.3:c.2044+144G>A	XP_006712782.1:n.2044+144G>A
XM_011511705.2:c.2044+144G>A	XP_011510007.1:n.2044+144G>A
NM_003151.4:c.2044+144G>A MANE Select	NP_003142.1:n.2044+144G>A
NM_001243835.2:c.2044+144G>A	NP_001230764.1:n.2044+144G>A