Canonical Allele Identifier: CA368965518

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299636G>A (hg19) ; chr7:g.114659581G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659581G>A , CM000669.2:g.114659581G>A	GRCh38
NC_000007.13:g.114299636G>A , CM000669.1:g.114299636G>A	GRCh37
NC_000007.12:g.114086872G>A	NCBI36
NG_007491.2:g.578272G>A
NG_007491.3:g.578272G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1606G>A	ENSP00000385069.4:p.Glu536Lys
ENST00000703612.1:c.1546G>A	ENSP00000515396.1:p.Glu516Lys
ENST00000703613.1:c.1606G>A	ENSP00000515397.1:p.Glu536Lys
ENST00000703614.1:c.1555G>A	ENSP00000515398.1:p.Glu519Lys
ENST00000703616.1:c.1681G>A	ENSP00000515400.1:p.Glu561Lys
ENST00000703617.1:c.1000G>A	ENSP00000515401.1:p.Glu334Lys
ENST00000703618.1:c.545-2484G>A
ENST00000350908.9:c.1555G>A MANE Select	ENSP00000265436.7:p.Glu519Lys
ENST00000393489.8:c.*1349G>A	ENSP00000377129.4:n.*1349G>A
ENST00000350908.8:c.1555G>A	ENSP00000265436.7:p.Glu519Lys
ENST00000393489.7:c.1279G>A	ENSP00000377129.3:p.Glu427Lys
ENST00000393491.7:c.1000G>A	ENSP00000377130.3:p.Glu334Lys
ENST00000393494.6:c.1555G>A	ENSP00000377132.2:p.Glu519Lys
ENST00000393498.6:c.1492G>A	ENSP00000377135.2:p.Glu498Lys
ENST00000403559.8:c.1606G>A	ENSP00000385069.4:p.Glu536Lys
ENST00000408937.7:c.1630G>A	ENSP00000386200.3:p.Glu544Lys
ENST00000412402.5:c.*1273G>A	ENSP00000405470.1:n.*1273G>A
ENST00000441290.6:c.*1555G>A	ENSP00000416825.1:n.*1555G>A
ENST00000634411.1:c.1504G>A	ENSP00000489135.1:p.Glu502Lys
ENST00000634623.1:c.1495G>A	ENSP00000488944.1:p.Glu499Lys
ENST00000635109.1:c.*1352G>A	ENSP00000489457.1:n.*1352G>A
ENST00000635534.1:c.1546G>A	ENSP00000489229.1:p.Glu516Lys
ENST00000635638.1:c.1558G>A	ENSP00000489073.1:p.Glu520Lys
NM_001172766.2:c.1552G>A	NP_001166237.1:p.Glu518Lys
NM_014491.3:c.1555G>A	NP_055306.1:p.Glu519Lys
NM_148898.3:c.1630G>A	NP_683696.2:p.Glu544Lys
NM_148900.3:c.1606G>A	NP_683698.2:p.Glu536Lys
NR_033766.1:n.1940G>A
NR_033767.1:n.1987G>A
XM_011516706.1:c.1699G>A	XP_011515008.1:p.Glu567Lys
XM_017012801.2:c.1630G>A	XP_016868290.1:p.Glu544Lys
NM_014491.4:c.1555G>A MANE Select	NP_055306.1:p.Glu519Lys
NM_001172766.3:c.1552G>A	NP_001166237.1:p.Glu518Lys
NM_148898.4:c.1630G>A	NP_683696.2:p.Glu544Lys
NR_033766.2:n.1923G>A
NR_033767.2:n.2169G>A
NM_148900.4:c.1606G>A	NP_683698.2:p.Glu536Lys