Canonical Allele Identifier: CA364069908
Gene: FOXP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1472670
dbSNP Id: rs2127404974

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41594873G>A , CM000668.2:g.41594873G>A GRCh38
NC_000006.11:g.41562611G>A , CM000668.1:g.41562611G>A GRCh37
NC_000006.10:g.41670589G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000704756.1:c.1540G>A ENSP00000516024.1:p.Ala514Thr
ENST00000307972.10:c.1540G>A MANE Select ENSP00000309823.4:p.Ala514Thr
ENST00000307972.8:c.1540G>A ENSP00000309823.4:p.Ala514Thr
ENST00000373057.7:c.1534G>A ENSP00000362148.3:p.Ala512Thr
ENST00000373060.5:c.1540G>A ENSP00000362151.1:p.Ala514Thr
ENST00000373063.7:c.1501G>A ENSP00000362154.3:p.Ala501Thr
ENST00000409208.5:c.1504G>A ENSP00000386958.1:p.Ala502Thr
NM_001012426.1:c.1540G>A NP_001012426.1:p.Ala514Thr
NM_001012427.1:c.1534G>A NP_001012427.1:p.Ala512Thr
NM_138457.2:c.1501G>A NP_612466.1:p.Ala501Thr
XM_006714991.2:c.1537G>A XP_006715054.1:p.Ala513Thr
XM_006714992.2:c.1522G>A XP_006715055.1:p.Ala508Thr
XM_011514289.1:c.1561G>A XP_011512591.1:p.Ala521Thr
XM_011514290.1:c.1555G>A XP_011512592.1:p.Ala519Thr
XM_011514291.1:c.1525G>A XP_011512593.1:p.Ala509Thr
XM_011514292.1:c.1465G>A XP_011512594.1:p.Ala489Thr
XM_011514293.1:c.1243G>A XP_011512595.1:p.Ala415Thr
XM_006714991.3:c.1537G>A XP_006715054.1:p.Ala513Thr
XM_011514289.2:c.1561G>A XP_011512591.1:p.Ala521Thr
XM_011514290.2:c.1555G>A XP_011512592.1:p.Ala519Thr
XM_011514291.3:c.1525G>A XP_011512593.1:p.Ala509Thr
XM_011514292.3:c.1465G>A XP_011512594.1:p.Ala489Thr
XM_011514293.3:c.1243G>A XP_011512595.1:p.Ala415Thr
XM_017010233.1:c.1561G>A XP_016865722.1:p.Ala521Thr
XM_017010234.2:c.1561G>A XP_016865723.1:p.Ala521Thr
XM_024446319.1:c.1504G>A XP_024302087.1:p.Ala502Thr
NM_001012427.2:c.1534G>A NP_001012427.1:p.Ala512Thr
NM_138457.3:c.1501G>A NP_612466.1:p.Ala501Thr
NM_001012426.2:c.1540G>A MANE Select NP_001012426.1:p.Ala514Thr