Canonical Allele Identifier: CA12323515

Gene: FOXP4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41568689C>T , CM000668.2:g.41568689C>T	GRCh38
NC_000006.11:g.41536427C>T , CM000668.1:g.41536427C>T	GRCh37
NC_000006.10:g.41644405C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704756.1:c.204+2725C>T	ENSP00000516024.1:n.204+2725C>T
ENST00000307972.10:c.204+2725C>T MANE Select	ENSP00000309823.4:n.204+2725C>T
ENST00000307972.8:c.204+2725C>T	ENSP00000309823.4:n.204+2725C>T
ENST00000373057.7:c.204+2725C>T	ENSP00000362148.3:n.204+2725C>T
ENST00000373060.5:c.204+2725C>T	ENSP00000362151.1:n.204+2725C>T
ENST00000373063.7:c.204+2725C>T	ENSP00000362154.3:n.204+2725C>T
ENST00000409208.5:c.204+2725C>T	ENSP00000386958.1:n.204+2725C>T
NM_001012426.1:c.204+2725C>T	NP_001012426.1:n.204+2725C>T
NM_001012427.1:c.204+2725C>T	NP_001012427.1:n.204+2725C>T
NM_138457.2:c.204+2725C>T	NP_612466.1:n.204+2725C>T
XM_006714991.2:c.204+2725C>T	XP_006715054.1:n.204+2725C>T
XM_006714992.2:c.204+2725C>T	XP_006715055.1:n.204+2725C>T
XM_011514289.1:c.204+2725C>T	XP_011512591.1:n.204+2725C>T
XM_011514290.1:c.204+2725C>T	XP_011512592.1:n.204+2725C>T
XM_011514291.1:c.204+2725C>T	XP_011512593.1:n.204+2725C>T
XM_011514292.1:c.204+2725C>T	XP_011512594.1:n.204+2725C>T
XR_926052.1:n.545+2725C>T
XR_926053.1:n.546+2725C>T
XM_006714991.3:c.204+2725C>T	XP_006715054.1:n.204+2725C>T
XM_011514289.2:c.204+2725C>T	XP_011512591.1:n.204+2725C>T
XM_011514290.2:c.204+2725C>T	XP_011512592.1:n.204+2725C>T
XM_011514291.3:c.204+2725C>T	XP_011512593.1:n.204+2725C>T
XM_011514292.3:c.204+2725C>T	XP_011512594.1:n.204+2725C>T
XM_017010233.1:c.204+2725C>T	XP_016865722.1:n.204+2725C>T
XM_017010234.2:c.204+2725C>T	XP_016865723.1:n.204+2725C>T
XM_024446319.1:c.204+2725C>T	XP_024302087.1:n.204+2725C>T
XR_926052.3:n.543+2725C>T
XR_926053.2:n.543+2725C>T
NM_001012427.2:c.204+2725C>T	NP_001012427.1:n.204+2725C>T
NM_138457.3:c.204+2725C>T	NP_612466.1:n.204+2725C>T
NM_001012426.2:c.204+2725C>T MANE Select	NP_001012426.1:n.204+2725C>T