Canonical Allele Identifier: CA368965616

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299677C>A (hg19) ; chr7:g.114659622C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659622C>A , CM000669.2:g.114659622C>A	GRCh38
NC_000007.13:g.114299677C>A , CM000669.1:g.114299677C>A	GRCh37
NC_000007.12:g.114086913C>A	NCBI36
NG_007491.2:g.578313C>A
NG_007491.3:g.578313C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1647C>A	ENSP00000385069.4:p.Ser549Arg
ENST00000703612.1:c.1587C>A	ENSP00000515396.1:p.Ser529Arg
ENST00000703613.1:c.1647C>A	ENSP00000515397.1:p.Ser549Arg
ENST00000703614.1:c.1596C>A	ENSP00000515398.1:p.Ser532Arg
ENST00000703616.1:c.1722C>A	ENSP00000515400.1:p.Ser574Arg
ENST00000703617.1:c.1041C>A	ENSP00000515401.1:p.Ser347Arg
ENST00000703618.1:c.545-2443C>A
ENST00000350908.9:c.1596C>A MANE Select	ENSP00000265436.7:p.Ser532Arg
ENST00000393489.8:c.*1390C>A	ENSP00000377129.4:n.*1390C>A
ENST00000350908.8:c.1596C>A	ENSP00000265436.7:p.Ser532Arg
ENST00000393489.7:c.1320C>A	ENSP00000377129.3:p.Ser440Arg
ENST00000393491.7:c.1041C>A	ENSP00000377130.3:p.Ser347Arg
ENST00000393494.6:c.1596C>A	ENSP00000377132.2:p.Ser532Arg
ENST00000393498.6:c.1533C>A	ENSP00000377135.2:p.Ser511Arg
ENST00000403559.8:c.1647C>A	ENSP00000385069.4:p.Ser549Arg
ENST00000408937.7:c.1671C>A	ENSP00000386200.3:p.Ser557Arg
ENST00000412402.5:c.*1314C>A	ENSP00000405470.1:n.*1314C>A
ENST00000441290.6:c.*1596C>A	ENSP00000416825.1:n.*1596C>A
ENST00000634411.1:c.1545C>A	ENSP00000489135.1:p.Ser515Arg
ENST00000634623.1:c.1536C>A	ENSP00000488944.1:p.Ser512Arg
ENST00000635109.1:c.*1393C>A	ENSP00000489457.1:n.*1393C>A
ENST00000635534.1:c.1587C>A	ENSP00000489229.1:p.Ser529Arg
ENST00000635638.1:c.1599C>A	ENSP00000489073.1:p.Ser533Arg
NM_001172766.2:c.1593C>A	NP_001166237.1:p.Ser531Arg
NM_014491.3:c.1596C>A	NP_055306.1:p.Ser532Arg
NM_148898.3:c.1671C>A	NP_683696.2:p.Ser557Arg
NM_148900.3:c.1647C>A	NP_683698.2:p.Ser549Arg
NR_033766.1:n.1981C>A
NR_033767.1:n.2028C>A
XM_011516706.1:c.1740C>A	XP_011515008.1:p.Ser580Arg
XM_017012801.2:c.1671C>A	XP_016868290.1:p.Ser557Arg
NM_014491.4:c.1596C>A MANE Select	NP_055306.1:p.Ser532Arg
NM_001172766.3:c.1593C>A	NP_001166237.1:p.Ser531Arg
NM_148898.4:c.1671C>A	NP_683696.2:p.Ser557Arg
NR_033766.2:n.1964C>A
NR_033767.2:n.2210C>A
NM_148900.4:c.1647C>A	NP_683698.2:p.Ser549Arg