Canonical Allele Identifier: CA368965797

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302142G>T (hg19) ; chr7:g.114662087G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662087G>T , CM000669.2:g.114662087G>T	GRCh38
NC_000007.13:g.114302142G>T , CM000669.1:g.114302142G>T	GRCh37
NC_000007.12:g.114089378G>T	NCBI36
NG_007491.2:g.580778G>T
NG_007491.3:g.580778G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1721G>T	ENSP00000385069.4:p.Ser574Ile
ENST00000703612.1:c.1661G>T	ENSP00000515396.1:p.Ser554Ile
ENST00000703613.1:c.1721G>T	ENSP00000515397.1:p.Ser574Ile
ENST00000703614.1:c.1670G>T	ENSP00000515398.1:p.Ser557Ile
ENST00000703616.1:c.1796G>T	ENSP00000515400.1:p.Ser599Ile
ENST00000703617.1:c.1115G>T	ENSP00000515401.1:p.Ser372Ile
ENST00000703618.1:c.567G>T
ENST00000350908.9:c.1670G>T MANE Select	ENSP00000265436.7:p.Ser557Ile
ENST00000393489.8:c.*1464G>T	ENSP00000377129.4:n.*1464G>T
ENST00000350908.8:c.1670G>T	ENSP00000265436.7:p.Ser557Ile
ENST00000393489.7:c.1394G>T	ENSP00000377129.3:p.Ser465Ile
ENST00000393491.7:c.1115G>T	ENSP00000377130.3:p.Ser372Ile
ENST00000393494.6:c.1670G>T	ENSP00000377132.2:p.Ser557Ile
ENST00000393498.6:c.1607G>T	ENSP00000377135.2:p.Ser536Ile
ENST00000403559.8:c.1721G>T	ENSP00000385069.4:p.Ser574Ile
ENST00000408937.7:c.1745G>T	ENSP00000386200.3:p.Ser582Ile
ENST00000412402.5:c.*1388G>T	ENSP00000405470.1:n.*1388G>T
ENST00000441290.6:c.*1670G>T	ENSP00000416825.1:n.*1670G>T
ENST00000634411.1:c.1619G>T	ENSP00000489135.1:p.Ser540Ile
ENST00000634623.1:c.1610G>T	ENSP00000488944.1:p.Ser537Ile
ENST00000634664.1:n.145G>T
ENST00000635109.1:c.*1467G>T	ENSP00000489457.1:n.*1467G>T
ENST00000635534.1:c.1661G>T	ENSP00000489229.1:p.Ser554Ile
ENST00000635638.1:c.1673G>T	ENSP00000489073.1:p.Ser558Ile
NM_001172766.2:c.1667G>T	NP_001166237.1:p.Ser556Ile
NM_014491.3:c.1670G>T	NP_055306.1:p.Ser557Ile
NM_148898.3:c.1745G>T	NP_683696.2:p.Ser582Ile
NM_148900.3:c.1721G>T	NP_683698.2:p.Ser574Ile
NR_033766.1:n.2055G>T
NR_033767.1:n.2102G>T
XM_011516706.1:c.1814G>T	XP_011515008.1:p.Ser605Ile
XM_017012801.2:c.1745G>T	XP_016868290.1:p.Ser582Ile
NM_014491.4:c.1670G>T MANE Select	NP_055306.1:p.Ser557Ile
NM_001172766.3:c.1667G>T	NP_001166237.1:p.Ser556Ile
NM_148898.4:c.1745G>T	NP_683696.2:p.Ser582Ile
NR_033766.2:n.2038G>T
NR_033767.2:n.2284G>T
NM_148900.4:c.1721G>T	NP_683698.2:p.Ser574Ile