Canonical Allele Identifier: CA368965751

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302121A>T (hg19) ; chr7:g.114662066A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662066A>T , CM000669.2:g.114662066A>T	GRCh38
NC_000007.13:g.114302121A>T , CM000669.1:g.114302121A>T	GRCh37
NC_000007.12:g.114089357A>T	NCBI36
NG_007491.2:g.580757A>T
NG_007491.3:g.580757A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1700A>T	ENSP00000385069.4:p.Asn567Ile
ENST00000703612.1:c.1640A>T	ENSP00000515396.1:p.Asn547Ile
ENST00000703613.1:c.1700A>T	ENSP00000515397.1:p.Asn567Ile
ENST00000703614.1:c.1649A>T	ENSP00000515398.1:p.Asn550Ile
ENST00000703616.1:c.1775A>T	ENSP00000515400.1:p.Asn592Ile
ENST00000703617.1:c.1094A>T	ENSP00000515401.1:p.Asn365Ile
ENST00000703618.1:c.546A>T
ENST00000350908.9:c.1649A>T MANE Select	ENSP00000265436.7:p.Asn550Ile
ENST00000393489.8:c.*1443A>T	ENSP00000377129.4:n.*1443A>T
ENST00000350908.8:c.1649A>T	ENSP00000265436.7:p.Asn550Ile
ENST00000393489.7:c.1373A>T	ENSP00000377129.3:p.Asn458Ile
ENST00000393491.7:c.1094A>T	ENSP00000377130.3:p.Asn365Ile
ENST00000393494.6:c.1649A>T	ENSP00000377132.2:p.Asn550Ile
ENST00000393498.6:c.1586A>T	ENSP00000377135.2:p.Asn529Ile
ENST00000403559.8:c.1700A>T	ENSP00000385069.4:p.Asn567Ile
ENST00000408937.7:c.1724A>T	ENSP00000386200.3:p.Asn575Ile
ENST00000412402.5:c.*1367A>T	ENSP00000405470.1:n.*1367A>T
ENST00000441290.6:c.*1649A>T	ENSP00000416825.1:n.*1649A>T
ENST00000634411.1:c.1598A>T	ENSP00000489135.1:p.Asn533Ile
ENST00000634623.1:c.1589A>T	ENSP00000488944.1:p.Asn530Ile
ENST00000634664.1:n.124A>T
ENST00000635109.1:c.*1446A>T	ENSP00000489457.1:n.*1446A>T
ENST00000635534.1:c.1640A>T	ENSP00000489229.1:p.Asn547Ile
ENST00000635638.1:c.1652A>T	ENSP00000489073.1:p.Asn551Ile
NM_001172766.2:c.1646A>T	NP_001166237.1:p.Asn549Ile
NM_014491.3:c.1649A>T	NP_055306.1:p.Asn550Ile
NM_148898.3:c.1724A>T	NP_683696.2:p.Asn575Ile
NM_148900.3:c.1700A>T	NP_683698.2:p.Asn567Ile
NR_033766.1:n.2034A>T
NR_033767.1:n.2081A>T
XM_011516706.1:c.1793A>T	XP_011515008.1:p.Asn598Ile
XM_017012801.2:c.1724A>T	XP_016868290.1:p.Asn575Ile
NM_014491.4:c.1649A>T MANE Select	NP_055306.1:p.Asn550Ile
NM_001172766.3:c.1646A>T	NP_001166237.1:p.Asn549Ile
NM_148898.4:c.1724A>T	NP_683696.2:p.Asn575Ile
NR_033766.2:n.2017A>T
NR_033767.2:n.2263A>T
NM_148900.4:c.1700A>T	NP_683698.2:p.Asn567Ile