Canonical Allele Identifier: CA368965538

Gene: FOXP2

Linked Data

• dbSNP Id: rs1806765942
• MyVariant Identifiers: chr7:g.114299645G>A (hg19) ; chr7:g.114659590G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659590G>A , CM000669.2:g.114659590G>A	GRCh38
NC_000007.13:g.114299645G>A , CM000669.1:g.114299645G>A	GRCh37
NC_000007.12:g.114086881G>A	NCBI36
NG_007491.2:g.578281G>A
NG_007491.3:g.578281G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1615G>A	ENSP00000385069.4:p.Asp539Asn
ENST00000703612.1:c.1555G>A	ENSP00000515396.1:p.Asp519Asn
ENST00000703613.1:c.1615G>A	ENSP00000515397.1:p.Asp539Asn
ENST00000703614.1:c.1564G>A	ENSP00000515398.1:p.Asp522Asn
ENST00000703616.1:c.1690G>A	ENSP00000515400.1:p.Asp564Asn
ENST00000703617.1:c.1009G>A	ENSP00000515401.1:p.Asp337Asn
ENST00000703618.1:c.545-2475G>A
ENST00000350908.9:c.1564G>A MANE Select	ENSP00000265436.7:p.Asp522Asn
ENST00000393489.8:c.*1358G>A	ENSP00000377129.4:n.*1358G>A
ENST00000350908.8:c.1564G>A	ENSP00000265436.7:p.Asp522Asn
ENST00000393489.7:c.1288G>A	ENSP00000377129.3:p.Asp430Asn
ENST00000393491.7:c.1009G>A	ENSP00000377130.3:p.Asp337Asn
ENST00000393494.6:c.1564G>A	ENSP00000377132.2:p.Asp522Asn
ENST00000393498.6:c.1501G>A	ENSP00000377135.2:p.Asp501Asn
ENST00000403559.8:c.1615G>A	ENSP00000385069.4:p.Asp539Asn
ENST00000408937.7:c.1639G>A	ENSP00000386200.3:p.Asp547Asn
ENST00000412402.5:c.*1282G>A	ENSP00000405470.1:n.*1282G>A
ENST00000441290.6:c.*1564G>A	ENSP00000416825.1:n.*1564G>A
ENST00000634411.1:c.1513G>A	ENSP00000489135.1:p.Asp505Asn
ENST00000634623.1:c.1504G>A	ENSP00000488944.1:p.Asp502Asn
ENST00000635109.1:c.*1361G>A	ENSP00000489457.1:n.*1361G>A
ENST00000635534.1:c.1555G>A	ENSP00000489229.1:p.Asp519Asn
ENST00000635638.1:c.1567G>A	ENSP00000489073.1:p.Asp523Asn
NM_001172766.2:c.1561G>A	NP_001166237.1:p.Asp521Asn
NM_014491.3:c.1564G>A	NP_055306.1:p.Asp522Asn
NM_148898.3:c.1639G>A	NP_683696.2:p.Asp547Asn
NM_148900.3:c.1615G>A	NP_683698.2:p.Asp539Asn
NR_033766.1:n.1949G>A
NR_033767.1:n.1996G>A
XM_011516706.1:c.1708G>A	XP_011515008.1:p.Asp570Asn
XM_017012801.2:c.1639G>A	XP_016868290.1:p.Asp547Asn
NM_014491.4:c.1564G>A MANE Select	NP_055306.1:p.Asp522Asn
NM_001172766.3:c.1561G>A	NP_001166237.1:p.Asp521Asn
NM_148898.4:c.1639G>A	NP_683696.2:p.Asp547Asn
NR_033766.2:n.1932G>A
NR_033767.2:n.2178G>A
NM_148900.4:c.1615G>A	NP_683698.2:p.Asp539Asn