Canonical Allele Identifier: CA500061266

Gene: STAT3

Linked Data

• dbSNP Id: rs2144694728
• MyVariant Identifiers: chr17:g.40475161C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42323143C>T , CM000679.2:g.42323143C>T	GRCh38
NC_000017.10:g.40475161C>T , CM000679.1:g.40475161C>T	GRCh37
NC_000017.9:g.37728687C>T	NCBI36
NG_007370.1:g.70353G>A , LRG_112:g.70353G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713583.1:c.1749G>A	ENSP00000518875.1:p.Gly583=
ENST00000264657.10:c.1749G>A MANE Select	ENSP00000264657.4:p.Gly583=
ENST00000676636.1:c.*141G>A	ENSP00000504255.1:n.*141G>A
ENST00000677002.1:c.1722G>A	ENSP00000503742.1:p.Lys574=
ENST00000677030.1:c.1749G>A	ENSP00000503662.1:p.Gly583=
ENST00000677152.1:c.1749G>A	ENSP00000502874.1:p.Gly583=
ENST00000677270.1:n.1202G>A
ENST00000677271.1:c.*137G>A	ENSP00000503912.1:n.*137G>A
ENST00000677308.1:c.*141G>A	ENSP00000503059.1:n.*141G>A
ENST00000677421.1:c.1845G>A	ENSP00000503599.1:p.Gly615=
ENST00000677442.1:c.1722G>A	ENSP00000504350.1:p.Lys574=
ENST00000677479.1:c.1749G>A	ENSP00000503559.1:p.Gly583=
ENST00000677603.1:c.1749G>A	ENSP00000504324.1:p.Gly583=
ENST00000677723.1:c.1749G>A	ENSP00000503574.1:p.Gly583=
ENST00000677763.1:n.1949G>A
ENST00000677820.1:c.*141G>A	ENSP00000504715.1:n.*141G>A
ENST00000678043.1:c.1728G>A	ENSP00000503872.1:p.Gly576=
ENST00000678044.1:c.1749G>A	ENSP00000503102.1:p.Gly583=
ENST00000678048.1:c.1665G>A	ENSP00000503799.1:p.Gly555=
ENST00000678445.1:c.*141G>A	ENSP00000503105.1:n.*141G>A
ENST00000678535.1:c.1749G>A	ENSP00000504081.1:p.Gly583=
ENST00000678572.1:c.1764G>A	ENSP00000504182.1:p.Gly588=
ENST00000678659.1:n.2186G>A
ENST00000678674.1:c.1653G>A	ENSP00000504062.1:p.Gly551=
ENST00000678764.1:n.2166G>A
ENST00000678792.1:c.1764G>A	ENSP00000504435.1:p.Gly588=
ENST00000678827.1:c.1749G>A	ENSP00000503634.1:p.Gly583=
ENST00000678905.1:c.1764G>A	ENSP00000503333.1:p.Gly588=
ENST00000678906.1:c.1749G>A	ENSP00000504184.1:p.Gly583=
ENST00000678913.1:c.1764G>A	ENSP00000504609.1:p.Gly588=
ENST00000678960.1:c.1749G>A	ENSP00000503181.1:p.Gly583=
ENST00000679014.1:c.1749G>A	ENSP00000503237.1:p.Gly583=
ENST00000679166.1:c.1665G>A	ENSP00000503308.1:p.Gly555=
ENST00000679185.1:c.1749G>A	ENSP00000503332.1:p.Gly583=
ENST00000679231.1:n.1992G>A
ENST00000264657.9:c.1749G>A	ENSP00000264657.4:p.Gly583=
ENST00000389272.7:c.1455G>A	ENSP00000373923.3:p.Gly485=
ENST00000404395.3:c.1749G>A	ENSP00000384943.3:p.Gly583=
ENST00000471989.5:n.718G>A
ENST00000498330.1:n.480G>A
ENST00000585517.5:c.1749G>A	ENSP00000467000.1:p.Gly583=
ENST00000588969.5:c.1749G>A	ENSP00000467985.1:p.Gly583=
NM_003150.3:c.1749G>A	NP_003141.2:p.Gly583=
NM_139276.2:c.1749G>A , LRG_112t1:c.1749G>A	NP_644805.1:p.Gly583=
NM_213662.1:c.1749G>A	NP_998827.1:p.Gly583=
XM_005257616.2:c.1749G>A	XP_005257673.2:p.Gly583=
XM_005257617.2:c.1749G>A	XP_005257674.2:p.Gly583=
XM_011525145.1:c.1749G>A	XP_011523447.1:p.Gly583=
XM_011525146.1:c.1749G>A	XP_011523448.1:p.Gly583=
XM_005257616.4:c.1749G>A	XP_005257673.2:p.Gly583=
XM_005257617.3:c.1749G>A	XP_005257674.2:p.Gly583=
XM_011525145.3:c.1749G>A	XP_011523447.1:p.Gly583=
XM_011525146.3:c.1749G>A	XP_011523448.1:p.Gly583=
XM_017024972.1:c.1749G>A	XP_016880461.1:p.Gly583=
XM_017024973.2:c.1749G>A	XP_016880462.1:p.Gly583=
XM_017024974.1:c.1749G>A	XP_016880463.1:p.Gly583=
XM_017024975.1:c.1749G>A	XP_016880464.1:p.Gly583=
XM_017024976.1:c.1749G>A	XP_016880465.1:p.Gly583=
XM_024450896.1:c.1845G>A	XP_024306664.1:p.Gly615=
NM_001369512.1:c.1749G>A	NP_001356441.1:p.Gly583=
NM_001369513.1:c.1749G>A	NP_001356442.1:p.Gly583=
NM_001369514.1:c.1749G>A	NP_001356443.1:p.Gly583=
NM_001369516.1:c.1749G>A	NP_001356445.1:p.Gly583=
NM_001369517.1:c.1749G>A	NP_001356446.1:p.Gly583=
NM_001369518.1:c.1749G>A	NP_001356447.1:p.Gly583=
NM_001369519.1:c.1749G>A	NP_001356448.1:p.Gly583=
NM_001369520.1:c.1749G>A	NP_001356449.1:p.Gly583=
NM_003150.4:c.1749G>A	NP_003141.2:p.Gly583=
NM_213662.2:c.1749G>A	NP_998827.1:p.Gly583=
NM_001384984.1:c.1665G>A	NP_001371913.1:p.Gly555=
NM_001384985.1:c.1671G>A	NP_001371914.1:p.Gly557=
NM_001384986.1:c.1764G>A	NP_001371915.1:p.Gly588=
NM_001384987.1:c.1728G>A	NP_001371916.1:p.Gly576=
NM_001384988.1:c.1749G>A	NP_001371917.1:p.Gly583=
NM_001384989.1:c.1653G>A	NP_001371918.1:p.Gly551=
NM_001384990.1:c.1764G>A	NP_001371919.1:p.Gly588=
NM_001384991.1:c.1722G>A	NP_001371920.1:p.Lys574=
NM_001384992.1:c.1689G>A	NP_001371921.1:p.Gly563=
NM_001384993.1:c.1749G>A	NP_001371922.1:p.Gly583=
NM_139276.3:c.1749G>A MANE Select	NP_644805.1:p.Gly583=