Canonical Allele Identifier: CA457220083

Gene: FOXP2

Linked Data

• gnomAD v4: 7-114659598-G-A
• MyVariant Identifiers: chr7:g.114299653G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659598G>A , CM000669.2:g.114659598G>A	GRCh38
NC_000007.13:g.114299653G>A , CM000669.1:g.114299653G>A	GRCh37
NC_000007.12:g.114086889G>A	NCBI36
NG_007491.2:g.578289G>A
NG_007491.3:g.578289G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1623G>A	ENSP00000385069.4:p.Gln541=
ENST00000703612.1:c.1563G>A	ENSP00000515396.1:p.Gln521=
ENST00000703613.1:c.1623G>A	ENSP00000515397.1:p.Gln541=
ENST00000703614.1:c.1572G>A	ENSP00000515398.1:p.Gln524=
ENST00000703616.1:c.1698G>A	ENSP00000515400.1:p.Gln566=
ENST00000703617.1:c.1017G>A	ENSP00000515401.1:p.Gln339=
ENST00000703618.1:c.545-2467G>A
ENST00000350908.9:c.1572G>A MANE Select	ENSP00000265436.7:p.Gln524=
ENST00000393489.8:c.*1366G>A	ENSP00000377129.4:n.*1366G>A
ENST00000350908.8:c.1572G>A	ENSP00000265436.7:p.Gln524=
ENST00000393489.7:c.1296G>A	ENSP00000377129.3:p.Gln432=
ENST00000393491.7:c.1017G>A	ENSP00000377130.3:p.Gln339=
ENST00000393494.6:c.1572G>A	ENSP00000377132.2:p.Gln524=
ENST00000393498.6:c.1509G>A	ENSP00000377135.2:p.Gln503=
ENST00000403559.8:c.1623G>A	ENSP00000385069.4:p.Gln541=
ENST00000408937.7:c.1647G>A	ENSP00000386200.3:p.Gln549=
ENST00000412402.5:c.*1290G>A	ENSP00000405470.1:n.*1290G>A
ENST00000441290.6:c.*1572G>A	ENSP00000416825.1:n.*1572G>A
ENST00000634411.1:c.1521G>A	ENSP00000489135.1:p.Gln507=
ENST00000634623.1:c.1512G>A	ENSP00000488944.1:p.Gln504=
ENST00000635109.1:c.*1369G>A	ENSP00000489457.1:n.*1369G>A
ENST00000635534.1:c.1563G>A	ENSP00000489229.1:p.Gln521=
ENST00000635638.1:c.1575G>A	ENSP00000489073.1:p.Gln525=
NM_001172766.2:c.1569G>A	NP_001166237.1:p.Gln523=
NM_014491.3:c.1572G>A	NP_055306.1:p.Gln524=
NM_148898.3:c.1647G>A	NP_683696.2:p.Gln549=
NM_148900.3:c.1623G>A	NP_683698.2:p.Gln541=
NR_033766.1:n.1957G>A
NR_033767.1:n.2004G>A
XM_011516706.1:c.1716G>A	XP_011515008.1:p.Gln572=
XM_017012801.2:c.1647G>A	XP_016868290.1:p.Gln549=
NM_014491.4:c.1572G>A MANE Select	NP_055306.1:p.Gln524=
NM_001172766.3:c.1569G>A	NP_001166237.1:p.Gln523=
NM_148898.4:c.1647G>A	NP_683696.2:p.Gln549=
NR_033766.2:n.1940G>A
NR_033767.2:n.2186G>A
NM_148900.4:c.1623G>A	NP_683698.2:p.Gln541=