Canonical Allele Identifier: CA368965716

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299721C>T (hg19) ; chr7:g.114659666C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659666C>T , CM000669.2:g.114659666C>T	GRCh38
NC_000007.13:g.114299721C>T , CM000669.1:g.114299721C>T	GRCh37
NC_000007.12:g.114086957C>T	NCBI36
NG_007491.2:g.578357C>T
NG_007491.3:g.578357C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1691C>T	ENSP00000385069.4:p.Thr564Ile
ENST00000703612.1:c.1631C>T	ENSP00000515396.1:p.Thr544Ile
ENST00000703613.1:c.1691C>T	ENSP00000515397.1:p.Thr564Ile
ENST00000703614.1:c.1640C>T	ENSP00000515398.1:p.Thr547Ile
ENST00000703616.1:c.1766C>T	ENSP00000515400.1:p.Thr589Ile
ENST00000703617.1:c.1085C>T	ENSP00000515401.1:p.Thr362Ile
ENST00000703618.1:c.545-2399C>T
ENST00000350908.9:c.1640C>T MANE Select	ENSP00000265436.7:p.Thr547Ile
ENST00000393489.8:c.*1434C>T	ENSP00000377129.4:n.*1434C>T
ENST00000350908.8:c.1640C>T	ENSP00000265436.7:p.Thr547Ile
ENST00000393489.7:c.1364C>T	ENSP00000377129.3:p.Thr455Ile
ENST00000393491.7:c.1085C>T	ENSP00000377130.3:p.Thr362Ile
ENST00000393494.6:c.1640C>T	ENSP00000377132.2:p.Thr547Ile
ENST00000393498.6:c.1577C>T	ENSP00000377135.2:p.Thr526Ile
ENST00000403559.8:c.1691C>T	ENSP00000385069.4:p.Thr564Ile
ENST00000408937.7:c.1715C>T	ENSP00000386200.3:p.Thr572Ile
ENST00000412402.5:c.*1358C>T	ENSP00000405470.1:n.*1358C>T
ENST00000441290.6:c.*1640C>T	ENSP00000416825.1:n.*1640C>T
ENST00000634411.1:c.1589C>T	ENSP00000489135.1:p.Thr530Ile
ENST00000634623.1:c.1580C>T	ENSP00000488944.1:p.Thr527Ile
ENST00000635109.1:c.*1437C>T	ENSP00000489457.1:n.*1437C>T
ENST00000635534.1:c.1631C>T	ENSP00000489229.1:p.Thr544Ile
ENST00000635638.1:c.1643C>T	ENSP00000489073.1:p.Thr548Ile
NM_001172766.2:c.1637C>T	NP_001166237.1:p.Thr546Ile
NM_014491.3:c.1640C>T	NP_055306.1:p.Thr547Ile
NM_148898.3:c.1715C>T	NP_683696.2:p.Thr572Ile
NM_148900.3:c.1691C>T	NP_683698.2:p.Thr564Ile
NR_033766.1:n.2025C>T
NR_033767.1:n.2072C>T
XM_011516706.1:c.1784C>T	XP_011515008.1:p.Thr595Ile
XM_017012801.2:c.1715C>T	XP_016868290.1:p.Thr572Ile
NM_014491.4:c.1640C>T MANE Select	NP_055306.1:p.Thr547Ile
NM_001172766.3:c.1637C>T	NP_001166237.1:p.Thr546Ile
NM_148898.4:c.1715C>T	NP_683696.2:p.Thr572Ile
NR_033766.2:n.2008C>T
NR_033767.2:n.2254C>T
NM_148900.4:c.1691C>T	NP_683698.2:p.Thr564Ile