Canonical Allele Identifier: CA457220281

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302222A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662167A>C , CM000669.2:g.114662167A>C	GRCh38
NC_000007.13:g.114302222A>C , CM000669.1:g.114302222A>C	GRCh37
NC_000007.12:g.114089458A>C	NCBI36
NG_007491.2:g.580858A>C
NG_007491.3:g.580858A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1801A>C	ENSP00000385069.4:p.Arg601=
ENST00000703612.1:c.1741A>C	ENSP00000515396.1:p.Arg581=
ENST00000703613.1:c.1801A>C	ENSP00000515397.1:p.Arg601=
ENST00000703614.1:c.1750A>C	ENSP00000515398.1:p.Arg584=
ENST00000703616.1:c.1876A>C	ENSP00000515400.1:p.Arg626=
ENST00000703617.1:c.1195A>C	ENSP00000515401.1:p.Arg399=
ENST00000703618.1:c.647A>C
ENST00000350908.9:c.1750A>C MANE Select	ENSP00000265436.7:p.Arg584=
ENST00000393489.8:c.*1544A>C	ENSP00000377129.4:n.*1544A>C
ENST00000350908.8:c.1750A>C	ENSP00000265436.7:p.Arg584=
ENST00000393489.7:c.1474A>C	ENSP00000377129.3:p.Arg492=
ENST00000393491.7:c.1195A>C	ENSP00000377130.3:p.Arg399=
ENST00000393494.6:c.1750A>C	ENSP00000377132.2:p.Arg584=
ENST00000393498.6:c.1687A>C	ENSP00000377135.2:p.Arg563=
ENST00000403559.8:c.1801A>C	ENSP00000385069.4:p.Arg601=
ENST00000408937.7:c.1825A>C	ENSP00000386200.3:p.Arg609=
ENST00000412402.5:c.*1468A>C	ENSP00000405470.1:n.*1468A>C
ENST00000441290.6:c.*1750A>C	ENSP00000416825.1:n.*1750A>C
ENST00000634411.1:c.1699A>C	ENSP00000489135.1:p.Arg567=
ENST00000634623.1:c.1690A>C	ENSP00000488944.1:p.Arg564=
ENST00000634664.1:n.225A>C
ENST00000635109.1:c.*1547A>C	ENSP00000489457.1:n.*1547A>C
ENST00000635534.1:c.1741A>C	ENSP00000489229.1:p.Arg581=
ENST00000635638.1:c.1753A>C	ENSP00000489073.1:p.Arg585=
NM_001172766.2:c.1747A>C	NP_001166237.1:p.Arg583=
NM_014491.3:c.1750A>C	NP_055306.1:p.Arg584=
NM_148898.3:c.1825A>C	NP_683696.2:p.Arg609=
NM_148900.3:c.1801A>C	NP_683698.2:p.Arg601=
NR_033766.1:n.2135A>C
NR_033767.1:n.2182A>C
XM_011516706.1:c.1894A>C	XP_011515008.1:p.Arg632=
XM_017012801.2:c.1825A>C	XP_016868290.1:p.Arg609=
NM_014491.4:c.1750A>C MANE Select	NP_055306.1:p.Arg584=
NM_001172766.3:c.1747A>C	NP_001166237.1:p.Arg583=
NM_148898.4:c.1825A>C	NP_683696.2:p.Arg609=
NR_033766.2:n.2118A>C
NR_033767.2:n.2364A>C
NM_148900.4:c.1801A>C	NP_683698.2:p.Arg601=