Canonical Allele Identifier: CA368965615

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299676G>T (hg19) ; chr7:g.114659621G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659621G>T , CM000669.2:g.114659621G>T	GRCh38
NC_000007.13:g.114299676G>T , CM000669.1:g.114299676G>T	GRCh37
NC_000007.12:g.114086912G>T	NCBI36
NG_007491.2:g.578312G>T
NG_007491.3:g.578312G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1646G>T	ENSP00000385069.4:p.Ser549Ile
ENST00000703612.1:c.1586G>T	ENSP00000515396.1:p.Ser529Ile
ENST00000703613.1:c.1646G>T	ENSP00000515397.1:p.Ser549Ile
ENST00000703614.1:c.1595G>T	ENSP00000515398.1:p.Ser532Ile
ENST00000703616.1:c.1721G>T	ENSP00000515400.1:p.Ser574Ile
ENST00000703617.1:c.1040G>T	ENSP00000515401.1:p.Ser347Ile
ENST00000703618.1:c.545-2444G>T
ENST00000350908.9:c.1595G>T MANE Select	ENSP00000265436.7:p.Ser532Ile
ENST00000393489.8:c.*1389G>T	ENSP00000377129.4:n.*1389G>T
ENST00000350908.8:c.1595G>T	ENSP00000265436.7:p.Ser532Ile
ENST00000393489.7:c.1319G>T	ENSP00000377129.3:p.Ser440Ile
ENST00000393491.7:c.1040G>T	ENSP00000377130.3:p.Ser347Ile
ENST00000393494.6:c.1595G>T	ENSP00000377132.2:p.Ser532Ile
ENST00000393498.6:c.1532G>T	ENSP00000377135.2:p.Ser511Ile
ENST00000403559.8:c.1646G>T	ENSP00000385069.4:p.Ser549Ile
ENST00000408937.7:c.1670G>T	ENSP00000386200.3:p.Ser557Ile
ENST00000412402.5:c.*1313G>T	ENSP00000405470.1:n.*1313G>T
ENST00000441290.6:c.*1595G>T	ENSP00000416825.1:n.*1595G>T
ENST00000634411.1:c.1544G>T	ENSP00000489135.1:p.Ser515Ile
ENST00000634623.1:c.1535G>T	ENSP00000488944.1:p.Ser512Ile
ENST00000635109.1:c.*1392G>T	ENSP00000489457.1:n.*1392G>T
ENST00000635534.1:c.1586G>T	ENSP00000489229.1:p.Ser529Ile
ENST00000635638.1:c.1598G>T	ENSP00000489073.1:p.Ser533Ile
NM_001172766.2:c.1592G>T	NP_001166237.1:p.Ser531Ile
NM_014491.3:c.1595G>T	NP_055306.1:p.Ser532Ile
NM_148898.3:c.1670G>T	NP_683696.2:p.Ser557Ile
NM_148900.3:c.1646G>T	NP_683698.2:p.Ser549Ile
NR_033766.1:n.1980G>T
NR_033767.1:n.2027G>T
XM_011516706.1:c.1739G>T	XP_011515008.1:p.Ser580Ile
XM_017012801.2:c.1670G>T	XP_016868290.1:p.Ser557Ile
NM_014491.4:c.1595G>T MANE Select	NP_055306.1:p.Ser532Ile
NM_001172766.3:c.1592G>T	NP_001166237.1:p.Ser531Ile
NM_148898.4:c.1670G>T	NP_683696.2:p.Ser557Ile
NR_033766.2:n.1963G>T
NR_033767.2:n.2209G>T
NM_148900.4:c.1646G>T	NP_683698.2:p.Ser549Ile