Canonical Allele Identifier: CA4446148

Gene: FOXP2

Linked Data

• dbSNP Id: rs781512446
• ExAC: 7:114299719 A / T
• gnomAD v4: 7-114659664-A-T
• MyVariant Identifiers: chr7:g.114299719A>T (hg19) ; chr7:g.114659664A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659664A>T , CM000669.2:g.114659664A>T	GRCh38
NC_000007.13:g.114299719A>T , CM000669.1:g.114299719A>T	GRCh37
NC_000007.12:g.114086955A>T	NCBI36
NG_007491.2:g.578355A>T
NG_007491.3:g.578355A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1689A>T	ENSP00000385069.4:p.Ala563=
ENST00000703612.1:c.1629A>T	ENSP00000515396.1:p.Ala543=
ENST00000703613.1:c.1689A>T	ENSP00000515397.1:p.Ala563=
ENST00000703614.1:c.1638A>T	ENSP00000515398.1:p.Ala546=
ENST00000703616.1:c.1764A>T	ENSP00000515400.1:p.Ala588=
ENST00000703617.1:c.1083A>T	ENSP00000515401.1:p.Ala361=
ENST00000703618.1:c.545-2401A>T
ENST00000350908.9:c.1638A>T MANE Select	ENSP00000265436.7:p.Ala546=
ENST00000393489.8:c.*1432A>T	ENSP00000377129.4:n.*1432A>T
ENST00000350908.8:c.1638A>T	ENSP00000265436.7:p.Ala546=
ENST00000393489.7:c.1362A>T	ENSP00000377129.3:p.Ala454=
ENST00000393491.7:c.1083A>T	ENSP00000377130.3:p.Ala361=
ENST00000393494.6:c.1638A>T	ENSP00000377132.2:p.Ala546=
ENST00000393498.6:c.1575A>T	ENSP00000377135.2:p.Ala525=
ENST00000403559.8:c.1689A>T	ENSP00000385069.4:p.Ala563=
ENST00000408937.7:c.1713A>T	ENSP00000386200.3:p.Ala571=
ENST00000412402.5:c.*1356A>T	ENSP00000405470.1:n.*1356A>T
ENST00000441290.6:c.*1638A>T	ENSP00000416825.1:n.*1638A>T
ENST00000634411.1:c.1587A>T	ENSP00000489135.1:p.Ala529=
ENST00000634623.1:c.1578A>T	ENSP00000488944.1:p.Ala526=
ENST00000635109.1:c.*1435A>T	ENSP00000489457.1:n.*1435A>T
ENST00000635534.1:c.1629A>T	ENSP00000489229.1:p.Ala543=
ENST00000635638.1:c.1641A>T	ENSP00000489073.1:p.Ala547=
NM_001172766.2:c.1635A>T	NP_001166237.1:p.Ala545=
NM_014491.3:c.1638A>T	NP_055306.1:p.Ala546=
NM_148898.3:c.1713A>T	NP_683696.2:p.Ala571=
NM_148900.3:c.1689A>T	NP_683698.2:p.Ala563=
NR_033766.1:n.2023A>T
NR_033767.1:n.2070A>T
XM_011516706.1:c.1782A>T	XP_011515008.1:p.Ala594=
XM_017012801.2:c.1713A>T	XP_016868290.1:p.Ala571=
NM_014491.4:c.1638A>T MANE Select	NP_055306.1:p.Ala546=
NM_001172766.3:c.1635A>T	NP_001166237.1:p.Ala545=
NM_148898.4:c.1713A>T	NP_683696.2:p.Ala571=
NR_033766.2:n.2006A>T
NR_033767.2:n.2252A>T
NM_148900.4:c.1689A>T	NP_683698.2:p.Ala563=