Canonical Allele Identifier: CA457220139

Gene: FOXP2

Linked Data

• gnomAD v4: 7-114659649-C-T
• MyVariant Identifiers: chr7:g.114299704C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659649C>T , CM000669.2:g.114659649C>T	GRCh38
NC_000007.13:g.114299704C>T , CM000669.1:g.114299704C>T	GRCh37
NC_000007.12:g.114086940C>T	NCBI36
NG_007491.2:g.578340C>T
NG_007491.3:g.578340C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1674C>T	ENSP00000385069.4:p.Phe558=
ENST00000703612.1:c.1614C>T	ENSP00000515396.1:p.Phe538=
ENST00000703613.1:c.1674C>T	ENSP00000515397.1:p.Phe558=
ENST00000703614.1:c.1623C>T	ENSP00000515398.1:p.Phe541=
ENST00000703616.1:c.1749C>T	ENSP00000515400.1:p.Phe583=
ENST00000703617.1:c.1068C>T	ENSP00000515401.1:p.Phe356=
ENST00000703618.1:c.545-2416C>T
ENST00000350908.9:c.1623C>T MANE Select	ENSP00000265436.7:p.Phe541=
ENST00000393489.8:c.*1417C>T	ENSP00000377129.4:n.*1417C>T
ENST00000350908.8:c.1623C>T	ENSP00000265436.7:p.Phe541=
ENST00000393489.7:c.1347C>T	ENSP00000377129.3:p.Phe449=
ENST00000393491.7:c.1068C>T	ENSP00000377130.3:p.Phe356=
ENST00000393494.6:c.1623C>T	ENSP00000377132.2:p.Phe541=
ENST00000393498.6:c.1560C>T	ENSP00000377135.2:p.Phe520=
ENST00000403559.8:c.1674C>T	ENSP00000385069.4:p.Phe558=
ENST00000408937.7:c.1698C>T	ENSP00000386200.3:p.Phe566=
ENST00000412402.5:c.*1341C>T	ENSP00000405470.1:n.*1341C>T
ENST00000441290.6:c.*1623C>T	ENSP00000416825.1:n.*1623C>T
ENST00000634411.1:c.1572C>T	ENSP00000489135.1:p.Phe524=
ENST00000634623.1:c.1563C>T	ENSP00000488944.1:p.Phe521=
ENST00000635109.1:c.*1420C>T	ENSP00000489457.1:n.*1420C>T
ENST00000635534.1:c.1614C>T	ENSP00000489229.1:p.Phe538=
ENST00000635638.1:c.1626C>T	ENSP00000489073.1:p.Phe542=
NM_001172766.2:c.1620C>T	NP_001166237.1:p.Phe540=
NM_014491.3:c.1623C>T	NP_055306.1:p.Phe541=
NM_148898.3:c.1698C>T	NP_683696.2:p.Phe566=
NM_148900.3:c.1674C>T	NP_683698.2:p.Phe558=
NR_033766.1:n.2008C>T
NR_033767.1:n.2055C>T
XM_011516706.1:c.1767C>T	XP_011515008.1:p.Phe589=
XM_017012801.2:c.1698C>T	XP_016868290.1:p.Phe566=
NM_014491.4:c.1623C>T MANE Select	NP_055306.1:p.Phe541=
NM_001172766.3:c.1620C>T	NP_001166237.1:p.Phe540=
NM_148898.4:c.1698C>T	NP_683696.2:p.Phe566=
NR_033766.2:n.1991C>T
NR_033767.2:n.2237C>T
NM_148900.4:c.1674C>T	NP_683698.2:p.Phe558=