Canonical Allele Identifier: CA3800867

Gene: FOXP4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41597844G>A , CM000668.2:g.41597844G>A	GRCh38
NC_000006.11:g.41565582G>A , CM000668.1:g.41565582G>A	GRCh37
NC_000006.10:g.41673560G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704756.1:c.1789G>A	ENSP00000516024.1:p.Ala597Thr
ENST00000307972.10:c.1789G>A MANE Select	ENSP00000309823.4:p.Ala597Thr
ENST00000307972.8:c.1789G>A	ENSP00000309823.4:p.Ala597Thr
ENST00000373057.7:c.1783G>A	ENSP00000362148.3:p.Ala595Thr
ENST00000373060.5:c.1789G>A	ENSP00000362151.1:p.Ala597Thr
ENST00000373063.7:c.1750G>A	ENSP00000362154.3:p.Ala584Thr
ENST00000409208.5:c.1753G>A	ENSP00000386958.1:p.Ala585Thr
NM_001012426.1:c.1789G>A	NP_001012426.1:p.Ala597Thr
NM_001012427.1:c.1783G>A	NP_001012427.1:p.Ala595Thr
NM_138457.2:c.1750G>A	NP_612466.1:p.Ala584Thr
XM_006714991.2:c.1786G>A	XP_006715054.1:p.Ala596Thr
XM_006714992.2:c.1771G>A	XP_006715055.1:p.Ala591Thr
XM_011514289.1:c.1810G>A	XP_011512591.1:p.Ala604Thr
XM_011514290.1:c.1804G>A	XP_011512592.1:p.Ala602Thr
XM_011514291.1:c.1774G>A	XP_011512593.1:p.Ala592Thr
XM_011514292.1:c.1714G>A	XP_011512594.1:p.Ala572Thr
XM_011514293.1:c.1492G>A	XP_011512595.1:p.Ala498Thr
XM_006714991.3:c.1786G>A	XP_006715054.1:p.Ala596Thr
XM_011514289.2:c.1810G>A	XP_011512591.1:p.Ala604Thr
XM_011514290.2:c.1804G>A	XP_011512592.1:p.Ala602Thr
XM_011514291.3:c.1774G>A	XP_011512593.1:p.Ala592Thr
XM_011514292.3:c.1714G>A	XP_011512594.1:p.Ala572Thr
XM_011514293.3:c.1492G>A	XP_011512595.1:p.Ala498Thr
XM_017010233.1:c.1810G>A	XP_016865722.1:p.Ala604Thr
XM_017010234.2:c.1810G>A	XP_016865723.1:p.Ala604Thr
XM_024446319.1:c.1753G>A	XP_024302087.1:p.Ala585Thr
NM_001012427.2:c.1783G>A	NP_001012427.1:p.Ala595Thr
NM_138457.3:c.1750G>A	NP_612466.1:p.Ala584Thr
NM_001012426.2:c.1789G>A MANE Select	NP_001012426.1:p.Ala597Thr