Canonical Allele Identifier: CA10639632
Gene: STAT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 323218
ClinVar RCV Id: RCV000323761
dbSNP Id: rs1053004

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42314074G>A , CM000679.2:g.42314074G>A GRCh38
NC_000017.10:g.40466092G>A , CM000679.1:g.40466092G>A GRCh37
NC_000017.9:g.37719618G>A NCBI36
NG_007370.1:g.79422C>T , LRG_112:g.79422C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264657.9:c.*1671C>T ENSP00000264657.4:p.=
NM_003150.3:c.*1671C>T NP_003141.2:p.=
NM_139276.2:c.*1671C>T , LRG_112t1:c.*1671C>T NP_644805.1:p.=
NM_213662.1:c.*1765C>T NP_998827.1:p.=
XM_005257616.2:c.*1671C>T XP_005257673.2:p.=
XM_005257617.2:c.*1671C>T XP_005257674.2:p.=
XM_011525145.1:c.*1671C>T XP_011523447.1:p.=
XM_011525146.1:c.*1765C>T XP_011523448.1:p.=
XM_011525145.3:c.*1671C>T XP_011523447.1:p.=
XM_011525146.3:c.*1765C>T XP_011523448.1:p.=
XM_017024973.2:c.*1765C>T XP_016880462.1:p.=
NM_001369512.1:c.*1671C>T NP_001356441.1:p.=
NM_001369513.1:c.*1671C>T NP_001356442.1:p.=
NM_001369514.1:c.*1671C>T NP_001356443.1:p.=
NM_001369516.1:c.*1671C>T NP_001356445.1:p.=
NM_001369517.1:c.*1765C>T NP_001356446.1:p.=
NM_001369518.1:c.*1765C>T NP_001356447.1:p.=
NM_001369519.1:c.*1765C>T NP_001356448.1:p.=
NM_001369520.1:c.*1765C>T NP_001356449.1:p.=
NM_003150.4:c.*1671C>T NP_003141.2:p.=
NM_213662.2:c.*1765C>T NP_998827.1:p.=
NM_001384984.1:c.*1671C>T NP_001371913.1:p.=
NM_001384985.1:c.*1671C>T NP_001371914.1:p.=
NM_001384986.1:c.*1765C>T NP_001371915.1:p.=
NM_001384987.1:c.*1671C>T NP_001371916.1:p.=
NM_001384988.1:c.*1671C>T NP_001371917.1:p.=
NM_001384989.1:c.*1671C>T NP_001371918.1:p.=
NM_001384990.1:c.*1765C>T NP_001371919.1:p.=
NM_001384991.1:c.*1671C>T NP_001371920.1:p.=
NM_001384992.1:c.*1671C>T NP_001371921.1:p.=
NM_001384993.1:c.*1671C>T NP_001371922.1:p.=
NM_139276.3:c.*1671C>T MANE Select NP_644805.1:p.=