Canonical Allele Identifier: CA368965775

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302133A>T (hg19) ; chr7:g.114662078A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662078A>T , CM000669.2:g.114662078A>T	GRCh38
NC_000007.13:g.114302133A>T , CM000669.1:g.114302133A>T	GRCh37
NC_000007.12:g.114089369A>T	NCBI36
NG_007491.2:g.580769A>T
NG_007491.3:g.580769A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1712A>T	ENSP00000385069.4:p.His571Leu
ENST00000703612.1:c.1652A>T	ENSP00000515396.1:p.His551Leu
ENST00000703613.1:c.1712A>T	ENSP00000515397.1:p.His571Leu
ENST00000703614.1:c.1661A>T	ENSP00000515398.1:p.His554Leu
ENST00000703616.1:c.1787A>T	ENSP00000515400.1:p.His596Leu
ENST00000703617.1:c.1106A>T	ENSP00000515401.1:p.His369Leu
ENST00000703618.1:c.558A>T
ENST00000350908.9:c.1661A>T MANE Select	ENSP00000265436.7:p.His554Leu
ENST00000393489.8:c.*1455A>T	ENSP00000377129.4:n.*1455A>T
ENST00000350908.8:c.1661A>T	ENSP00000265436.7:p.His554Leu
ENST00000393489.7:c.1385A>T	ENSP00000377129.3:p.His462Leu
ENST00000393491.7:c.1106A>T	ENSP00000377130.3:p.His369Leu
ENST00000393494.6:c.1661A>T	ENSP00000377132.2:p.His554Leu
ENST00000393498.6:c.1598A>T	ENSP00000377135.2:p.His533Leu
ENST00000403559.8:c.1712A>T	ENSP00000385069.4:p.His571Leu
ENST00000408937.7:c.1736A>T	ENSP00000386200.3:p.His579Leu
ENST00000412402.5:c.*1379A>T	ENSP00000405470.1:n.*1379A>T
ENST00000441290.6:c.*1661A>T	ENSP00000416825.1:n.*1661A>T
ENST00000634411.1:c.1610A>T	ENSP00000489135.1:p.His537Leu
ENST00000634623.1:c.1601A>T	ENSP00000488944.1:p.His534Leu
ENST00000634664.1:n.136A>T
ENST00000635109.1:c.*1458A>T	ENSP00000489457.1:n.*1458A>T
ENST00000635534.1:c.1652A>T	ENSP00000489229.1:p.His551Leu
ENST00000635638.1:c.1664A>T	ENSP00000489073.1:p.His555Leu
NM_001172766.2:c.1658A>T	NP_001166237.1:p.His553Leu
NM_014491.3:c.1661A>T	NP_055306.1:p.His554Leu
NM_148898.3:c.1736A>T	NP_683696.2:p.His579Leu
NM_148900.3:c.1712A>T	NP_683698.2:p.His571Leu
NR_033766.1:n.2046A>T
NR_033767.1:n.2093A>T
XM_011516706.1:c.1805A>T	XP_011515008.1:p.His602Leu
XM_017012801.2:c.1736A>T	XP_016868290.1:p.His579Leu
NM_014491.4:c.1661A>T MANE Select	NP_055306.1:p.His554Leu
NM_001172766.3:c.1658A>T	NP_001166237.1:p.His553Leu
NM_148898.4:c.1736A>T	NP_683696.2:p.His579Leu
NR_033766.2:n.2029A>T
NR_033767.2:n.2275A>T
NM_148900.4:c.1712A>T	NP_683698.2:p.His571Leu