Canonical Allele Identifier: CA3800529

Gene: FOXP4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41587454C>T , CM000668.2:g.41587454C>T	GRCh38
NC_000006.11:g.41555192C>T , CM000668.1:g.41555192C>T	GRCh37
NC_000006.10:g.41663170C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704756.1:c.814C>T	ENSP00000516024.1:p.Leu272Phe
ENST00000704757.1:n.346C>T
ENST00000307972.10:c.814C>T MANE Select	ENSP00000309823.4:p.Leu272Phe
ENST00000670130.1:c.475C>T	ENSP00000499606.1:p.Leu159Phe
ENST00000307972.8:c.814C>T	ENSP00000309823.4:p.Leu272Phe
ENST00000373057.7:c.808C>T	ENSP00000362148.3:p.Leu270Phe
ENST00000373060.5:c.814C>T	ENSP00000362151.1:p.Leu272Phe
ENST00000373063.7:c.811C>T	ENSP00000362154.3:p.Leu271Phe
ENST00000409208.5:c.814C>T	ENSP00000386958.1:p.Leu272Phe
NM_001012426.1:c.814C>T	NP_001012426.1:p.Leu272Phe
NM_001012427.1:c.808C>T	NP_001012427.1:p.Leu270Phe
NM_138457.2:c.811C>T	NP_612466.1:p.Leu271Phe
XM_006714991.2:c.811C>T	XP_006715054.1:p.Leu271Phe
XM_006714992.2:c.796C>T	XP_006715055.1:p.Leu266Phe
XM_011514289.1:c.835C>T	XP_011512591.1:p.Leu279Phe
XM_011514290.1:c.829C>T	XP_011512592.1:p.Leu277Phe
XM_011514291.1:c.835C>T	XP_011512593.1:p.Leu279Phe
XM_011514292.1:c.739C>T	XP_011512594.1:p.Leu247Phe
XM_011514293.1:c.517C>T	XP_011512595.1:p.Leu173Phe
XR_926052.1:n.1176C>T
XR_926053.1:n.1177C>T
XM_006714991.3:c.811C>T	XP_006715054.1:p.Leu271Phe
XM_011514289.2:c.835C>T	XP_011512591.1:p.Leu279Phe
XM_011514290.2:c.829C>T	XP_011512592.1:p.Leu277Phe
XM_011514291.3:c.835C>T	XP_011512593.1:p.Leu279Phe
XM_011514292.3:c.739C>T	XP_011512594.1:p.Leu247Phe
XM_011514293.3:c.517C>T	XP_011512595.1:p.Leu173Phe
XM_017010233.1:c.835C>T	XP_016865722.1:p.Leu279Phe
XM_017010234.2:c.835C>T	XP_016865723.1:p.Leu279Phe
XM_024446319.1:c.814C>T	XP_024302087.1:p.Leu272Phe
XR_926052.3:n.1174C>T
XR_926053.2:n.1174C>T
NM_001012427.2:c.808C>T	NP_001012427.1:p.Leu270Phe
NM_138457.3:c.811C>T	NP_612466.1:p.Leu271Phe
NM_001012426.2:c.814C>T MANE Select	NP_001012426.1:p.Leu272Phe