Canonical Allele Identifier: CA2607043893

Gene: STAT4

Linked Data

• gnomAD v3: 2-191038035-C-A
• gnomAD v4: 2-191038035-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191038035C>A , CM000664.2:g.191038035C>A	GRCh38
NC_000002.11:g.191902761C>A , CM000664.1:g.191902761C>A	GRCh37
NC_000002.10:g.191611006C>A	NCBI36
NG_012852.1:g.118165G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000392320.7:c.1434+1164G>T MANE Select	ENSP00000376134.2:n.1434+1164G>T
ENST00000358470.8:c.1434+1164G>T	ENSP00000351255.4:n.1434+1164G>T
ENST00000392320.6:c.1434+1164G>T	ENSP00000376134.2:n.1434+1164G>T
ENST00000470708.1:n.393+1164G>T
ENST00000495849.5:n.1502+1164G>T
NM_001243835.1:c.1434+1164G>T	NP_001230764.1:n.1434+1164G>T
NM_003151.3:c.1434+1164G>T	NP_003142.1:n.1434+1164G>T
XM_005246817.3:c.1461+1164G>T	XP_005246874.1:n.1461+1164G>T
XM_006712719.2:c.1434+1164G>T	XP_006712782.1:n.1434+1164G>T
XM_011511704.1:c.1461+1164G>T	XP_011510006.1:n.1461+1164G>T
XM_011511705.1:c.1434+1164G>T	XP_011510007.1:n.1434+1164G>T
XM_006712719.3:c.1434+1164G>T	XP_006712782.1:n.1434+1164G>T
XM_011511705.2:c.1434+1164G>T	XP_011510007.1:n.1434+1164G>T
NM_003151.4:c.1434+1164G>T MANE Select	NP_003142.1:n.1434+1164G>T
NM_001243835.2:c.1434+1164G>T	NP_001230764.1:n.1434+1164G>T