Canonical Allele Identifier: CA368965630

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299682T>A (hg19) ; chr7:g.114659627T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659627T>A , CM000669.2:g.114659627T>A	GRCh38
NC_000007.13:g.114299682T>A , CM000669.1:g.114299682T>A	GRCh37
NC_000007.12:g.114086918T>A	NCBI36
NG_007491.2:g.578318T>A
NG_007491.3:g.578318T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1652T>A	ENSP00000385069.4:p.Phe551Tyr
ENST00000703612.1:c.1592T>A	ENSP00000515396.1:p.Phe531Tyr
ENST00000703613.1:c.1652T>A	ENSP00000515397.1:p.Phe551Tyr
ENST00000703614.1:c.1601T>A	ENSP00000515398.1:p.Phe534Tyr
ENST00000703616.1:c.1727T>A	ENSP00000515400.1:p.Phe576Tyr
ENST00000703617.1:c.1046T>A	ENSP00000515401.1:p.Phe349Tyr
ENST00000703618.1:c.545-2438T>A
ENST00000350908.9:c.1601T>A MANE Select	ENSP00000265436.7:p.Phe534Tyr
ENST00000393489.8:c.*1395T>A	ENSP00000377129.4:n.*1395T>A
ENST00000350908.8:c.1601T>A	ENSP00000265436.7:p.Phe534Tyr
ENST00000393489.7:c.1325T>A	ENSP00000377129.3:p.Phe442Tyr
ENST00000393491.7:c.1046T>A	ENSP00000377130.3:p.Phe349Tyr
ENST00000393494.6:c.1601T>A	ENSP00000377132.2:p.Phe534Tyr
ENST00000393498.6:c.1538T>A	ENSP00000377135.2:p.Phe513Tyr
ENST00000403559.8:c.1652T>A	ENSP00000385069.4:p.Phe551Tyr
ENST00000408937.7:c.1676T>A	ENSP00000386200.3:p.Phe559Tyr
ENST00000412402.5:c.*1319T>A	ENSP00000405470.1:n.*1319T>A
ENST00000441290.6:c.*1601T>A	ENSP00000416825.1:n.*1601T>A
ENST00000634411.1:c.1550T>A	ENSP00000489135.1:p.Phe517Tyr
ENST00000634623.1:c.1541T>A	ENSP00000488944.1:p.Phe514Tyr
ENST00000635109.1:c.*1398T>A	ENSP00000489457.1:n.*1398T>A
ENST00000635534.1:c.1592T>A	ENSP00000489229.1:p.Phe531Tyr
ENST00000635638.1:c.1604T>A	ENSP00000489073.1:p.Phe535Tyr
NM_001172766.2:c.1598T>A	NP_001166237.1:p.Phe533Tyr
NM_014491.3:c.1601T>A	NP_055306.1:p.Phe534Tyr
NM_148898.3:c.1676T>A	NP_683696.2:p.Phe559Tyr
NM_148900.3:c.1652T>A	NP_683698.2:p.Phe551Tyr
NR_033766.1:n.1986T>A
NR_033767.1:n.2033T>A
XM_011516706.1:c.1745T>A	XP_011515008.1:p.Phe582Tyr
XM_017012801.2:c.1676T>A	XP_016868290.1:p.Phe559Tyr
NM_014491.4:c.1601T>A MANE Select	NP_055306.1:p.Phe534Tyr
NM_001172766.3:c.1598T>A	NP_001166237.1:p.Phe533Tyr
NM_148898.4:c.1676T>A	NP_683696.2:p.Phe559Tyr
NR_033766.2:n.1969T>A
NR_033767.2:n.2215T>A
NM_148900.4:c.1652T>A	NP_683698.2:p.Phe551Tyr