Canonical Allele Identifier: CA368965898

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302187T>C (hg19) ; chr7:g.114662132T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662132T>C , CM000669.2:g.114662132T>C	GRCh38
NC_000007.13:g.114302187T>C , CM000669.1:g.114302187T>C	GRCh37
NC_000007.12:g.114089423T>C	NCBI36
NG_007491.2:g.580823T>C
NG_007491.3:g.580823T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1766T>C	ENSP00000385069.4:p.Val589Ala
ENST00000703612.1:c.1706T>C	ENSP00000515396.1:p.Val569Ala
ENST00000703613.1:c.1766T>C	ENSP00000515397.1:p.Val589Ala
ENST00000703614.1:c.1715T>C	ENSP00000515398.1:p.Val572Ala
ENST00000703616.1:c.1841T>C	ENSP00000515400.1:p.Val614Ala
ENST00000703617.1:c.1160T>C	ENSP00000515401.1:p.Val387Ala
ENST00000703618.1:c.612T>C
ENST00000350908.9:c.1715T>C MANE Select	ENSP00000265436.7:p.Val572Ala
ENST00000393489.8:c.*1509T>C	ENSP00000377129.4:n.*1509T>C
ENST00000350908.8:c.1715T>C	ENSP00000265436.7:p.Val572Ala
ENST00000393489.7:c.1439T>C	ENSP00000377129.3:p.Val480Ala
ENST00000393491.7:c.1160T>C	ENSP00000377130.3:p.Val387Ala
ENST00000393494.6:c.1715T>C	ENSP00000377132.2:p.Val572Ala
ENST00000393498.6:c.1652T>C	ENSP00000377135.2:p.Val551Ala
ENST00000403559.8:c.1766T>C	ENSP00000385069.4:p.Val589Ala
ENST00000408937.7:c.1790T>C	ENSP00000386200.3:p.Val597Ala
ENST00000412402.5:c.*1433T>C	ENSP00000405470.1:n.*1433T>C
ENST00000441290.6:c.*1715T>C	ENSP00000416825.1:n.*1715T>C
ENST00000634411.1:c.1664T>C	ENSP00000489135.1:p.Val555Ala
ENST00000634623.1:c.1655T>C	ENSP00000488944.1:p.Val552Ala
ENST00000634664.1:n.190T>C
ENST00000635109.1:c.*1512T>C	ENSP00000489457.1:n.*1512T>C
ENST00000635534.1:c.1706T>C	ENSP00000489229.1:p.Val569Ala
ENST00000635638.1:c.1718T>C	ENSP00000489073.1:p.Val573Ala
NM_001172766.2:c.1712T>C	NP_001166237.1:p.Val571Ala
NM_014491.3:c.1715T>C	NP_055306.1:p.Val572Ala
NM_148898.3:c.1790T>C	NP_683696.2:p.Val597Ala
NM_148900.3:c.1766T>C	NP_683698.2:p.Val589Ala
NR_033766.1:n.2100T>C
NR_033767.1:n.2147T>C
XM_011516706.1:c.1859T>C	XP_011515008.1:p.Val620Ala
XM_017012801.2:c.1790T>C	XP_016868290.1:p.Val597Ala
NM_014491.4:c.1715T>C MANE Select	NP_055306.1:p.Val572Ala
NM_001172766.3:c.1712T>C	NP_001166237.1:p.Val571Ala
NM_148898.4:c.1790T>C	NP_683696.2:p.Val597Ala
NR_033766.2:n.2083T>C
NR_033767.2:n.2329T>C
NM_148900.4:c.1766T>C	NP_683698.2:p.Val589Ala