Canonical Allele Identifier: CA368965657

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299696G>A (hg19) ; chr7:g.114659641G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659641G>A , CM000669.2:g.114659641G>A	GRCh38
NC_000007.13:g.114299696G>A , CM000669.1:g.114299696G>A	GRCh37
NC_000007.12:g.114086932G>A	NCBI36
NG_007491.2:g.578332G>A
NG_007491.3:g.578332G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1666G>A	ENSP00000385069.4:p.Ala556Thr
ENST00000703612.1:c.1606G>A	ENSP00000515396.1:p.Ala536Thr
ENST00000703613.1:c.1666G>A	ENSP00000515397.1:p.Ala556Thr
ENST00000703614.1:c.1615G>A	ENSP00000515398.1:p.Ala539Thr
ENST00000703616.1:c.1741G>A	ENSP00000515400.1:p.Ala581Thr
ENST00000703617.1:c.1060G>A	ENSP00000515401.1:p.Ala354Thr
ENST00000703618.1:c.545-2424G>A
ENST00000350908.9:c.1615G>A MANE Select	ENSP00000265436.7:p.Ala539Thr
ENST00000393489.8:c.*1409G>A	ENSP00000377129.4:n.*1409G>A
ENST00000350908.8:c.1615G>A	ENSP00000265436.7:p.Ala539Thr
ENST00000393489.7:c.1339G>A	ENSP00000377129.3:p.Ala447Thr
ENST00000393491.7:c.1060G>A	ENSP00000377130.3:p.Ala354Thr
ENST00000393494.6:c.1615G>A	ENSP00000377132.2:p.Ala539Thr
ENST00000393498.6:c.1552G>A	ENSP00000377135.2:p.Ala518Thr
ENST00000403559.8:c.1666G>A	ENSP00000385069.4:p.Ala556Thr
ENST00000408937.7:c.1690G>A	ENSP00000386200.3:p.Ala564Thr
ENST00000412402.5:c.*1333G>A	ENSP00000405470.1:n.*1333G>A
ENST00000441290.6:c.*1615G>A	ENSP00000416825.1:n.*1615G>A
ENST00000634411.1:c.1564G>A	ENSP00000489135.1:p.Ala522Thr
ENST00000634623.1:c.1555G>A	ENSP00000488944.1:p.Ala519Thr
ENST00000635109.1:c.*1412G>A	ENSP00000489457.1:n.*1412G>A
ENST00000635534.1:c.1606G>A	ENSP00000489229.1:p.Ala536Thr
ENST00000635638.1:c.1618G>A	ENSP00000489073.1:p.Ala540Thr
NM_001172766.2:c.1612G>A	NP_001166237.1:p.Ala538Thr
NM_014491.3:c.1615G>A	NP_055306.1:p.Ala539Thr
NM_148898.3:c.1690G>A	NP_683696.2:p.Ala564Thr
NM_148900.3:c.1666G>A	NP_683698.2:p.Ala556Thr
NR_033766.1:n.2000G>A
NR_033767.1:n.2047G>A
XM_011516706.1:c.1759G>A	XP_011515008.1:p.Ala587Thr
XM_017012801.2:c.1690G>A	XP_016868290.1:p.Ala564Thr
NM_014491.4:c.1615G>A MANE Select	NP_055306.1:p.Ala539Thr
NM_001172766.3:c.1612G>A	NP_001166237.1:p.Ala538Thr
NM_148898.4:c.1690G>A	NP_683696.2:p.Ala564Thr
NR_033766.2:n.1983G>A
NR_033767.2:n.2229G>A
NM_148900.4:c.1666G>A	NP_683698.2:p.Ala556Thr