Canonical Allele Identifier: CA368965679

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299705A>T (hg19) ; chr7:g.114659650A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659650A>T , CM000669.2:g.114659650A>T	GRCh38
NC_000007.13:g.114299705A>T , CM000669.1:g.114299705A>T	GRCh37
NC_000007.12:g.114086941A>T	NCBI36
NG_007491.2:g.578341A>T
NG_007491.3:g.578341A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1675A>T	ENSP00000385069.4:p.Arg559Trp
ENST00000703612.1:c.1615A>T	ENSP00000515396.1:p.Arg539Trp
ENST00000703613.1:c.1675A>T	ENSP00000515397.1:p.Arg559Trp
ENST00000703614.1:c.1624A>T	ENSP00000515398.1:p.Arg542Trp
ENST00000703616.1:c.1750A>T	ENSP00000515400.1:p.Arg584Trp
ENST00000703617.1:c.1069A>T	ENSP00000515401.1:p.Arg357Trp
ENST00000703618.1:c.545-2415A>T
ENST00000350908.9:c.1624A>T MANE Select	ENSP00000265436.7:p.Arg542Trp
ENST00000393489.8:c.*1418A>T	ENSP00000377129.4:n.*1418A>T
ENST00000350908.8:c.1624A>T	ENSP00000265436.7:p.Arg542Trp
ENST00000393489.7:c.1348A>T	ENSP00000377129.3:p.Arg450Trp
ENST00000393491.7:c.1069A>T	ENSP00000377130.3:p.Arg357Trp
ENST00000393494.6:c.1624A>T	ENSP00000377132.2:p.Arg542Trp
ENST00000393498.6:c.1561A>T	ENSP00000377135.2:p.Arg521Trp
ENST00000403559.8:c.1675A>T	ENSP00000385069.4:p.Arg559Trp
ENST00000408937.7:c.1699A>T	ENSP00000386200.3:p.Arg567Trp
ENST00000412402.5:c.*1342A>T	ENSP00000405470.1:n.*1342A>T
ENST00000441290.6:c.*1624A>T	ENSP00000416825.1:n.*1624A>T
ENST00000634411.1:c.1573A>T	ENSP00000489135.1:p.Arg525Trp
ENST00000634623.1:c.1564A>T	ENSP00000488944.1:p.Arg522Trp
ENST00000635109.1:c.*1421A>T	ENSP00000489457.1:n.*1421A>T
ENST00000635534.1:c.1615A>T	ENSP00000489229.1:p.Arg539Trp
ENST00000635638.1:c.1627A>T	ENSP00000489073.1:p.Arg543Trp
NM_001172766.2:c.1621A>T	NP_001166237.1:p.Arg541Trp
NM_014491.3:c.1624A>T	NP_055306.1:p.Arg542Trp
NM_148898.3:c.1699A>T	NP_683696.2:p.Arg567Trp
NM_148900.3:c.1675A>T	NP_683698.2:p.Arg559Trp
NR_033766.1:n.2009A>T
NR_033767.1:n.2056A>T
XM_011516706.1:c.1768A>T	XP_011515008.1:p.Arg590Trp
XM_017012801.2:c.1699A>T	XP_016868290.1:p.Arg567Trp
NM_014491.4:c.1624A>T MANE Select	NP_055306.1:p.Arg542Trp
NM_001172766.3:c.1621A>T	NP_001166237.1:p.Arg541Trp
NM_148898.4:c.1699A>T	NP_683696.2:p.Arg567Trp
NR_033766.2:n.1992A>T
NR_033767.2:n.2238A>T
NM_148900.4:c.1675A>T	NP_683698.2:p.Arg559Trp