Canonical Allele Identifier: CA457220195

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302131T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662076T>A , CM000669.2:g.114662076T>A	GRCh38
NC_000007.13:g.114302131T>A , CM000669.1:g.114302131T>A	GRCh37
NC_000007.12:g.114089367T>A	NCBI36
NG_007491.2:g.580767T>A
NG_007491.3:g.580767T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1710T>A	ENSP00000385069.4:p.Arg570=
ENST00000703612.1:c.1650T>A	ENSP00000515396.1:p.Arg550=
ENST00000703613.1:c.1710T>A	ENSP00000515397.1:p.Arg570=
ENST00000703614.1:c.1659T>A	ENSP00000515398.1:p.Arg553=
ENST00000703616.1:c.1785T>A	ENSP00000515400.1:p.Arg595=
ENST00000703617.1:c.1104T>A	ENSP00000515401.1:p.Arg368=
ENST00000703618.1:c.556T>A
ENST00000350908.9:c.1659T>A MANE Select	ENSP00000265436.7:p.Arg553=
ENST00000393489.8:c.*1453T>A	ENSP00000377129.4:n.*1453T>A
ENST00000350908.8:c.1659T>A	ENSP00000265436.7:p.Arg553=
ENST00000393489.7:c.1383T>A	ENSP00000377129.3:p.Arg461=
ENST00000393491.7:c.1104T>A	ENSP00000377130.3:p.Arg368=
ENST00000393494.6:c.1659T>A	ENSP00000377132.2:p.Arg553=
ENST00000393498.6:c.1596T>A	ENSP00000377135.2:p.Arg532=
ENST00000403559.8:c.1710T>A	ENSP00000385069.4:p.Arg570=
ENST00000408937.7:c.1734T>A	ENSP00000386200.3:p.Arg578=
ENST00000412402.5:c.*1377T>A	ENSP00000405470.1:n.*1377T>A
ENST00000441290.6:c.*1659T>A	ENSP00000416825.1:n.*1659T>A
ENST00000634411.1:c.1608T>A	ENSP00000489135.1:p.Arg536=
ENST00000634623.1:c.1599T>A	ENSP00000488944.1:p.Arg533=
ENST00000634664.1:n.134T>A
ENST00000635109.1:c.*1456T>A	ENSP00000489457.1:n.*1456T>A
ENST00000635534.1:c.1650T>A	ENSP00000489229.1:p.Arg550=
ENST00000635638.1:c.1662T>A	ENSP00000489073.1:p.Arg554=
NM_001172766.2:c.1656T>A	NP_001166237.1:p.Arg552=
NM_014491.3:c.1659T>A	NP_055306.1:p.Arg553=
NM_148898.3:c.1734T>A	NP_683696.2:p.Arg578=
NM_148900.3:c.1710T>A	NP_683698.2:p.Arg570=
NR_033766.1:n.2044T>A
NR_033767.1:n.2091T>A
XM_011516706.1:c.1803T>A	XP_011515008.1:p.Arg601=
XM_017012801.2:c.1734T>A	XP_016868290.1:p.Arg578=
NM_014491.4:c.1659T>A MANE Select	NP_055306.1:p.Arg553=
NM_001172766.3:c.1656T>A	NP_001166237.1:p.Arg552=
NM_148898.4:c.1734T>A	NP_683696.2:p.Arg578=
NR_033766.2:n.2027T>A
NR_033767.2:n.2273T>A
NM_148900.4:c.1710T>A	NP_683698.2:p.Arg570=