Canonical Allele Identifier: CA368965926

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302199A>T (hg19) ; chr7:g.114662144A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662144A>T , CM000669.2:g.114662144A>T	GRCh38
NC_000007.13:g.114302199A>T , CM000669.1:g.114302199A>T	GRCh37
NC_000007.12:g.114089435A>T	NCBI36
NG_007491.2:g.580835A>T
NG_007491.3:g.580835A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1778A>T	ENSP00000385069.4:p.Asp593Val
ENST00000703612.1:c.1718A>T	ENSP00000515396.1:p.Asp573Val
ENST00000703613.1:c.1778A>T	ENSP00000515397.1:p.Asp593Val
ENST00000703614.1:c.1727A>T	ENSP00000515398.1:p.Asp576Val
ENST00000703616.1:c.1853A>T	ENSP00000515400.1:p.Asp618Val
ENST00000703617.1:c.1172A>T	ENSP00000515401.1:p.Asp391Val
ENST00000703618.1:c.624A>T
ENST00000350908.9:c.1727A>T MANE Select	ENSP00000265436.7:p.Asp576Val
ENST00000393489.8:c.*1521A>T	ENSP00000377129.4:n.*1521A>T
ENST00000350908.8:c.1727A>T	ENSP00000265436.7:p.Asp576Val
ENST00000393489.7:c.1451A>T	ENSP00000377129.3:p.Asp484Val
ENST00000393491.7:c.1172A>T	ENSP00000377130.3:p.Asp391Val
ENST00000393494.6:c.1727A>T	ENSP00000377132.2:p.Asp576Val
ENST00000393498.6:c.1664A>T	ENSP00000377135.2:p.Asp555Val
ENST00000403559.8:c.1778A>T	ENSP00000385069.4:p.Asp593Val
ENST00000408937.7:c.1802A>T	ENSP00000386200.3:p.Asp601Val
ENST00000412402.5:c.*1445A>T	ENSP00000405470.1:n.*1445A>T
ENST00000441290.6:c.*1727A>T	ENSP00000416825.1:n.*1727A>T
ENST00000634411.1:c.1676A>T	ENSP00000489135.1:p.Asp559Val
ENST00000634623.1:c.1667A>T	ENSP00000488944.1:p.Asp556Val
ENST00000634664.1:n.202A>T
ENST00000635109.1:c.*1524A>T	ENSP00000489457.1:n.*1524A>T
ENST00000635534.1:c.1718A>T	ENSP00000489229.1:p.Asp573Val
ENST00000635638.1:c.1730A>T	ENSP00000489073.1:p.Asp577Val
NM_001172766.2:c.1724A>T	NP_001166237.1:p.Asp575Val
NM_014491.3:c.1727A>T	NP_055306.1:p.Asp576Val
NM_148898.3:c.1802A>T	NP_683696.2:p.Asp601Val
NM_148900.3:c.1778A>T	NP_683698.2:p.Asp593Val
NR_033766.1:n.2112A>T
NR_033767.1:n.2159A>T
XM_011516706.1:c.1871A>T	XP_011515008.1:p.Asp624Val
XM_017012801.2:c.1802A>T	XP_016868290.1:p.Asp601Val
NM_014491.4:c.1727A>T MANE Select	NP_055306.1:p.Asp576Val
NM_001172766.3:c.1724A>T	NP_001166237.1:p.Asp575Val
NM_148898.4:c.1802A>T	NP_683696.2:p.Asp601Val
NR_033766.2:n.2095A>T
NR_033767.2:n.2341A>T
NM_148900.4:c.1778A>T	NP_683698.2:p.Asp593Val