Canonical Allele Identifier: CA457220228

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302164A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662109A>G , CM000669.2:g.114662109A>G	GRCh38
NC_000007.13:g.114302164A>G , CM000669.1:g.114302164A>G	GRCh37
NC_000007.12:g.114089400A>G	NCBI36
NG_007491.2:g.580800A>G
NG_007491.3:g.580800A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1743A>G	ENSP00000385069.4:p.Arg581=
ENST00000703612.1:c.1683A>G	ENSP00000515396.1:p.Arg561=
ENST00000703613.1:c.1743A>G	ENSP00000515397.1:p.Arg581=
ENST00000703614.1:c.1692A>G	ENSP00000515398.1:p.Arg564=
ENST00000703616.1:c.1818A>G	ENSP00000515400.1:p.Arg606=
ENST00000703617.1:c.1137A>G	ENSP00000515401.1:p.Arg379=
ENST00000703618.1:c.589A>G
ENST00000350908.9:c.1692A>G MANE Select	ENSP00000265436.7:p.Arg564=
ENST00000393489.8:c.*1486A>G	ENSP00000377129.4:n.*1486A>G
ENST00000350908.8:c.1692A>G	ENSP00000265436.7:p.Arg564=
ENST00000393489.7:c.1416A>G	ENSP00000377129.3:p.Arg472=
ENST00000393491.7:c.1137A>G	ENSP00000377130.3:p.Arg379=
ENST00000393494.6:c.1692A>G	ENSP00000377132.2:p.Arg564=
ENST00000393498.6:c.1629A>G	ENSP00000377135.2:p.Arg543=
ENST00000403559.8:c.1743A>G	ENSP00000385069.4:p.Arg581=
ENST00000408937.7:c.1767A>G	ENSP00000386200.3:p.Arg589=
ENST00000412402.5:c.*1410A>G	ENSP00000405470.1:n.*1410A>G
ENST00000441290.6:c.*1692A>G	ENSP00000416825.1:n.*1692A>G
ENST00000634411.1:c.1641A>G	ENSP00000489135.1:p.Arg547=
ENST00000634623.1:c.1632A>G	ENSP00000488944.1:p.Arg544=
ENST00000634664.1:n.167A>G
ENST00000635109.1:c.*1489A>G	ENSP00000489457.1:n.*1489A>G
ENST00000635534.1:c.1683A>G	ENSP00000489229.1:p.Arg561=
ENST00000635638.1:c.1695A>G	ENSP00000489073.1:p.Arg565=
NM_001172766.2:c.1689A>G	NP_001166237.1:p.Arg563=
NM_014491.3:c.1692A>G	NP_055306.1:p.Arg564=
NM_148898.3:c.1767A>G	NP_683696.2:p.Arg589=
NM_148900.3:c.1743A>G	NP_683698.2:p.Arg581=
NR_033766.1:n.2077A>G
NR_033767.1:n.2124A>G
XM_011516706.1:c.1836A>G	XP_011515008.1:p.Arg612=
XM_017012801.2:c.1767A>G	XP_016868290.1:p.Arg589=
NM_014491.4:c.1692A>G MANE Select	NP_055306.1:p.Arg564=
NM_001172766.3:c.1689A>G	NP_001166237.1:p.Arg563=
NM_148898.4:c.1767A>G	NP_683696.2:p.Arg589=
NR_033766.2:n.2060A>G
NR_033767.2:n.2306A>G
NM_148900.4:c.1743A>G	NP_683698.2:p.Arg581=