Canonical Allele Identifier: CA16607583

Gene: STAT3

Linked Data

• ClinVar Variation Id: 381595
• ClinVar RCV Id: RCV000417632 ; RCV002521588
• dbSNP Id: rs1057521091
• MyVariant Identifiers: chr17:g.40477048T>G (hg19) ; chr17:g.42325030T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42325030T>G , CM000679.2:g.42325030T>G	GRCh38
NC_000017.10:g.40477048T>G , CM000679.1:g.40477048T>G	GRCh37
NC_000017.9:g.37730574T>G	NCBI36
NG_007370.1:g.68466A>C , LRG_112:g.68466A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713583.1:c.1397A>C	ENSP00000518875.1:p.Asn466Thr
ENST00000264657.10:c.1397A>C MANE Select	ENSP00000264657.4:p.Asn466Thr
ENST00000676636.1:c.1397A>C	ENSP00000504255.1:p.Asn466Thr
ENST00000677002.1:c.1397A>C	ENSP00000503742.1:p.Asn466Thr
ENST00000677030.1:c.1397A>C	ENSP00000503662.1:p.Asn466Thr
ENST00000677152.1:c.1397A>C	ENSP00000502874.1:p.Asn466Thr
ENST00000677270.1:n.632A>C
ENST00000677271.1:c.1365+1086A>C	ENSP00000503912.1:n.1365+1086A>C
ENST00000677308.1:c.1397A>C	ENSP00000503059.1:p.Asn466Thr
ENST00000677421.1:c.1493A>C	ENSP00000503599.1:p.Asn498Thr
ENST00000677442.1:c.1397A>C	ENSP00000504350.1:p.Asn466Thr
ENST00000677479.1:c.1397A>C	ENSP00000503559.1:p.Asn466Thr
ENST00000677603.1:c.1397A>C	ENSP00000504324.1:p.Asn466Thr
ENST00000677723.1:c.1397A>C	ENSP00000503574.1:p.Asn466Thr
ENST00000677763.1:n.1597A>C
ENST00000677820.1:c.1397A>C	ENSP00000504715.1:p.Asn466Thr
ENST00000678043.1:c.1397A>C	ENSP00000503872.1:p.Asn466Thr
ENST00000678044.1:c.1397A>C	ENSP00000503102.1:p.Asn466Thr
ENST00000678048.1:c.1313A>C	ENSP00000503799.1:p.Asn438Thr
ENST00000678445.1:c.1397A>C	ENSP00000503105.1:p.Asn466Thr
ENST00000678535.1:c.1397A>C	ENSP00000504081.1:p.Asn466Thr
ENST00000678572.1:c.1412A>C	ENSP00000504182.1:p.Asn471Thr
ENST00000678659.1:n.1616A>C
ENST00000678674.1:c.1301A>C	ENSP00000504062.1:p.Asn434Thr
ENST00000678764.1:n.1596A>C
ENST00000678792.1:c.1412A>C	ENSP00000504435.1:p.Asn471Thr
ENST00000678827.1:c.1397A>C	ENSP00000503634.1:p.Asn466Thr
ENST00000678905.1:c.1412A>C	ENSP00000503333.1:p.Asn471Thr
ENST00000678906.1:c.1397A>C	ENSP00000504184.1:p.Asn466Thr
ENST00000678913.1:c.1412A>C	ENSP00000504609.1:p.Asn471Thr
ENST00000678960.1:c.1397A>C	ENSP00000503181.1:p.Asn466Thr
ENST00000679014.1:c.1397A>C	ENSP00000503237.1:p.Asn466Thr
ENST00000679166.1:c.1313A>C	ENSP00000503308.1:p.Asn438Thr
ENST00000679185.1:c.1397A>C	ENSP00000503332.1:p.Asn466Thr
ENST00000679231.1:n.1422A>C
ENST00000264657.9:c.1397A>C	ENSP00000264657.4:p.Asn466Thr
ENST00000389272.7:c.1103A>C	ENSP00000373923.3:p.Asn368Thr
ENST00000404395.3:c.1397A>C	ENSP00000384943.3:p.Asn466Thr
ENST00000471989.5:n.32A>C
ENST00000498330.1:n.128A>C
ENST00000585517.5:c.1397A>C	ENSP00000467000.1:p.Asn466Thr
ENST00000588969.5:c.1397A>C	ENSP00000467985.1:p.Asn466Thr
NM_003150.3:c.1397A>C	NP_003141.2:p.Asn466Thr
NM_139276.2:c.1397A>C , LRG_112t1:c.1397A>C	NP_644805.1:p.Asn466Thr
NM_213662.1:c.1397A>C	NP_998827.1:p.Asn466Thr
XM_005257616.2:c.1397A>C	XP_005257673.2:p.Asn466Thr
XM_005257617.2:c.1397A>C	XP_005257674.2:p.Asn466Thr
XM_011525145.1:c.1397A>C	XP_011523447.1:p.Asn466Thr
XM_011525146.1:c.1397A>C	XP_011523448.1:p.Asn466Thr
XM_005257616.4:c.1397A>C	XP_005257673.2:p.Asn466Thr
XM_005257617.3:c.1397A>C	XP_005257674.2:p.Asn466Thr
XM_011525145.3:c.1397A>C	XP_011523447.1:p.Asn466Thr
XM_011525146.3:c.1397A>C	XP_011523448.1:p.Asn466Thr
XM_017024972.1:c.1397A>C	XP_016880461.1:p.Asn466Thr
XM_017024973.2:c.1397A>C	XP_016880462.1:p.Asn466Thr
XM_017024974.1:c.1397A>C	XP_016880463.1:p.Asn466Thr
XM_017024975.1:c.1397A>C	XP_016880464.1:p.Asn466Thr
XM_017024976.1:c.1397A>C	XP_016880465.1:p.Asn466Thr
XM_024450896.1:c.1493A>C	XP_024306664.1:p.Asn498Thr
NM_001369512.1:c.1397A>C	NP_001356441.1:p.Asn466Thr
NM_001369513.1:c.1397A>C	NP_001356442.1:p.Asn466Thr
NM_001369514.1:c.1397A>C	NP_001356443.1:p.Asn466Thr
NM_001369516.1:c.1397A>C	NP_001356445.1:p.Asn466Thr
NM_001369517.1:c.1397A>C	NP_001356446.1:p.Asn466Thr
NM_001369518.1:c.1397A>C	NP_001356447.1:p.Asn466Thr
NM_001369519.1:c.1397A>C	NP_001356448.1:p.Asn466Thr
NM_001369520.1:c.1397A>C	NP_001356449.1:p.Asn466Thr
NM_003150.4:c.1397A>C	NP_003141.2:p.Asn466Thr
NM_213662.2:c.1397A>C	NP_998827.1:p.Asn466Thr
NM_001384984.1:c.1313A>C	NP_001371913.1:p.Asn438Thr
NM_001384985.1:c.1319A>C	NP_001371914.1:p.Asn440Thr
NM_001384986.1:c.1412A>C	NP_001371915.1:p.Asn471Thr
NM_001384987.1:c.1397A>C	NP_001371916.1:p.Asn466Thr
NM_001384988.1:c.1397A>C	NP_001371917.1:p.Asn466Thr
NM_001384989.1:c.1301A>C	NP_001371918.1:p.Asn434Thr
NM_001384990.1:c.1412A>C	NP_001371919.1:p.Asn471Thr
NM_001384991.1:c.1397A>C	NP_001371920.1:p.Asn466Thr
NM_001384992.1:c.1337A>C	NP_001371921.1:p.Asn446Thr
NM_001384993.1:c.1397A>C	NP_001371922.1:p.Asn466Thr
NM_139276.3:c.1397A>C MANE Select	NP_644805.1:p.Asn466Thr