Canonical Allele Identifier: CA3800866

Gene: FOXP4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41597843C>T , CM000668.2:g.41597843C>T	GRCh38
NC_000006.11:g.41565581C>T , CM000668.1:g.41565581C>T	GRCh37
NC_000006.10:g.41673559C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704756.1:c.1788C>T	ENSP00000516024.1:p.Ser596=
ENST00000307972.10:c.1788C>T MANE Select	ENSP00000309823.4:p.Ser596=
ENST00000307972.8:c.1788C>T	ENSP00000309823.4:p.Ser596=
ENST00000373057.7:c.1782C>T	ENSP00000362148.3:p.Ser594=
ENST00000373060.5:c.1788C>T	ENSP00000362151.1:p.Ser596=
ENST00000373063.7:c.1749C>T	ENSP00000362154.3:p.Ser583=
ENST00000409208.5:c.1752C>T	ENSP00000386958.1:p.Ser584=
NM_001012426.1:c.1788C>T	NP_001012426.1:p.Ser596=
NM_001012427.1:c.1782C>T	NP_001012427.1:p.Ser594=
NM_138457.2:c.1749C>T	NP_612466.1:p.Ser583=
XM_006714991.2:c.1785C>T	XP_006715054.1:p.Ser595=
XM_006714992.2:c.1770C>T	XP_006715055.1:p.Ser590=
XM_011514289.1:c.1809C>T	XP_011512591.1:p.Ser603=
XM_011514290.1:c.1803C>T	XP_011512592.1:p.Ser601=
XM_011514291.1:c.1773C>T	XP_011512593.1:p.Ser591=
XM_011514292.1:c.1713C>T	XP_011512594.1:p.Ser571=
XM_011514293.1:c.1491C>T	XP_011512595.1:p.Ser497=
XM_006714991.3:c.1785C>T	XP_006715054.1:p.Ser595=
XM_011514289.2:c.1809C>T	XP_011512591.1:p.Ser603=
XM_011514290.2:c.1803C>T	XP_011512592.1:p.Ser601=
XM_011514291.3:c.1773C>T	XP_011512593.1:p.Ser591=
XM_011514292.3:c.1713C>T	XP_011512594.1:p.Ser571=
XM_011514293.3:c.1491C>T	XP_011512595.1:p.Ser497=
XM_017010233.1:c.1809C>T	XP_016865722.1:p.Ser603=
XM_017010234.2:c.1809C>T	XP_016865723.1:p.Ser603=
XM_024446319.1:c.1752C>T	XP_024302087.1:p.Ser584=
NM_001012427.2:c.1782C>T	NP_001012427.1:p.Ser594=
NM_138457.3:c.1749C>T	NP_612466.1:p.Ser583=
NM_001012426.2:c.1788C>T MANE Select	NP_001012426.1:p.Ser596=