Canonical Allele Identifier: CA368965611

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299675A>T (hg19) ; chr7:g.114659620A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659620A>T , CM000669.2:g.114659620A>T	GRCh38
NC_000007.13:g.114299675A>T , CM000669.1:g.114299675A>T	GRCh37
NC_000007.12:g.114086911A>T	NCBI36
NG_007491.2:g.578311A>T
NG_007491.3:g.578311A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1645A>T	ENSP00000385069.4:p.Ser549Cys
ENST00000703612.1:c.1585A>T	ENSP00000515396.1:p.Ser529Cys
ENST00000703613.1:c.1645A>T	ENSP00000515397.1:p.Ser549Cys
ENST00000703614.1:c.1594A>T	ENSP00000515398.1:p.Ser532Cys
ENST00000703616.1:c.1720A>T	ENSP00000515400.1:p.Ser574Cys
ENST00000703617.1:c.1039A>T	ENSP00000515401.1:p.Ser347Cys
ENST00000703618.1:c.545-2445A>T
ENST00000350908.9:c.1594A>T MANE Select	ENSP00000265436.7:p.Ser532Cys
ENST00000393489.8:c.*1388A>T	ENSP00000377129.4:n.*1388A>T
ENST00000350908.8:c.1594A>T	ENSP00000265436.7:p.Ser532Cys
ENST00000393489.7:c.1318A>T	ENSP00000377129.3:p.Ser440Cys
ENST00000393491.7:c.1039A>T	ENSP00000377130.3:p.Ser347Cys
ENST00000393494.6:c.1594A>T	ENSP00000377132.2:p.Ser532Cys
ENST00000393498.6:c.1531A>T	ENSP00000377135.2:p.Ser511Cys
ENST00000403559.8:c.1645A>T	ENSP00000385069.4:p.Ser549Cys
ENST00000408937.7:c.1669A>T	ENSP00000386200.3:p.Ser557Cys
ENST00000412402.5:c.*1312A>T	ENSP00000405470.1:n.*1312A>T
ENST00000441290.6:c.*1594A>T	ENSP00000416825.1:n.*1594A>T
ENST00000634411.1:c.1543A>T	ENSP00000489135.1:p.Ser515Cys
ENST00000634623.1:c.1534A>T	ENSP00000488944.1:p.Ser512Cys
ENST00000635109.1:c.*1391A>T	ENSP00000489457.1:n.*1391A>T
ENST00000635534.1:c.1585A>T	ENSP00000489229.1:p.Ser529Cys
ENST00000635638.1:c.1597A>T	ENSP00000489073.1:p.Ser533Cys
NM_001172766.2:c.1591A>T	NP_001166237.1:p.Ser531Cys
NM_014491.3:c.1594A>T	NP_055306.1:p.Ser532Cys
NM_148898.3:c.1669A>T	NP_683696.2:p.Ser557Cys
NM_148900.3:c.1645A>T	NP_683698.2:p.Ser549Cys
NR_033766.1:n.1979A>T
NR_033767.1:n.2026A>T
XM_011516706.1:c.1738A>T	XP_011515008.1:p.Ser580Cys
XM_017012801.2:c.1669A>T	XP_016868290.1:p.Ser557Cys
NM_014491.4:c.1594A>T MANE Select	NP_055306.1:p.Ser532Cys
NM_001172766.3:c.1591A>T	NP_001166237.1:p.Ser531Cys
NM_148898.4:c.1669A>T	NP_683696.2:p.Ser557Cys
NR_033766.2:n.1962A>T
NR_033767.2:n.2208A>T
NM_148900.4:c.1645A>T	NP_683698.2:p.Ser549Cys