Canonical Allele Identifier: CA368965544

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299647C>A (hg19) ; chr7:g.114659592C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659592C>A , CM000669.2:g.114659592C>A	GRCh38
NC_000007.13:g.114299647C>A , CM000669.1:g.114299647C>A	GRCh37
NC_000007.12:g.114086883C>A	NCBI36
NG_007491.2:g.578283C>A
NG_007491.3:g.578283C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1617C>A	ENSP00000385069.4:p.Asp539Glu
ENST00000703612.1:c.1557C>A	ENSP00000515396.1:p.Asp519Glu
ENST00000703613.1:c.1617C>A	ENSP00000515397.1:p.Asp539Glu
ENST00000703614.1:c.1566C>A	ENSP00000515398.1:p.Asp522Glu
ENST00000703616.1:c.1692C>A	ENSP00000515400.1:p.Asp564Glu
ENST00000703617.1:c.1011C>A	ENSP00000515401.1:p.Asp337Glu
ENST00000703618.1:c.545-2473C>A
ENST00000350908.9:c.1566C>A MANE Select	ENSP00000265436.7:p.Asp522Glu
ENST00000393489.8:c.*1360C>A	ENSP00000377129.4:n.*1360C>A
ENST00000350908.8:c.1566C>A	ENSP00000265436.7:p.Asp522Glu
ENST00000393489.7:c.1290C>A	ENSP00000377129.3:p.Asp430Glu
ENST00000393491.7:c.1011C>A	ENSP00000377130.3:p.Asp337Glu
ENST00000393494.6:c.1566C>A	ENSP00000377132.2:p.Asp522Glu
ENST00000393498.6:c.1503C>A	ENSP00000377135.2:p.Asp501Glu
ENST00000403559.8:c.1617C>A	ENSP00000385069.4:p.Asp539Glu
ENST00000408937.7:c.1641C>A	ENSP00000386200.3:p.Asp547Glu
ENST00000412402.5:c.*1284C>A	ENSP00000405470.1:n.*1284C>A
ENST00000441290.6:c.*1566C>A	ENSP00000416825.1:n.*1566C>A
ENST00000634411.1:c.1515C>A	ENSP00000489135.1:p.Asp505Glu
ENST00000634623.1:c.1506C>A	ENSP00000488944.1:p.Asp502Glu
ENST00000635109.1:c.*1363C>A	ENSP00000489457.1:n.*1363C>A
ENST00000635534.1:c.1557C>A	ENSP00000489229.1:p.Asp519Glu
ENST00000635638.1:c.1569C>A	ENSP00000489073.1:p.Asp523Glu
NM_001172766.2:c.1563C>A	NP_001166237.1:p.Asp521Glu
NM_014491.3:c.1566C>A	NP_055306.1:p.Asp522Glu
NM_148898.3:c.1641C>A	NP_683696.2:p.Asp547Glu
NM_148900.3:c.1617C>A	NP_683698.2:p.Asp539Glu
NR_033766.1:n.1951C>A
NR_033767.1:n.1998C>A
XM_011516706.1:c.1710C>A	XP_011515008.1:p.Asp570Glu
XM_017012801.2:c.1641C>A	XP_016868290.1:p.Asp547Glu
NM_014491.4:c.1566C>A MANE Select	NP_055306.1:p.Asp522Glu
NM_001172766.3:c.1563C>A	NP_001166237.1:p.Asp521Glu
NM_148898.4:c.1641C>A	NP_683696.2:p.Asp547Glu
NR_033766.2:n.1934C>A
NR_033767.2:n.2180C>A
NM_148900.4:c.1617C>A	NP_683698.2:p.Asp539Glu