Canonical Allele Identifier: CA1736047808

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114661973_114661977delinsCTGAT , CM000669.2:g.114661973_114661977delinsCTGAT	GRCh38
NC_000007.13:g.114302028_114302032delinsCTGAT , CM000669.1:g.114302028_114302032delinsCTGAT	GRCh37
NC_000007.12:g.114089264_114089268delinsCTGAT	NCBI36
NG_007491.2:g.580664_580668delinsCTGAT
NG_007491.3:g.580664_580668delinsCTGAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1699-92_1699-88delinsCTGAT	ENSP00000385069.4:n.1699-92_1699-88delins...
ENST00000703612.1:c.1639-92_1639-88delinsCTGAT	ENSP00000515396.1:n.1639-92_1639-88delins...
ENST00000703613.1:c.1699-92_1699-88delinsCTGAT	ENSP00000515397.1:n.1699-92_1699-88delins...
ENST00000703614.1:c.1648-92_1648-88delinsCTGAT	ENSP00000515398.1:n.1648-92_1648-88delins...
ENST00000703616.1:c.1774-92_1774-88delinsCTGAT	ENSP00000515400.1:n.1774-92_1774-88delins...
ENST00000703617.1:c.1093-92_1093-88delinsCTGAT	ENSP00000515401.1:n.1093-92_1093-88delins...
ENST00000703618.1:c.545-92_545-88delinsCTGAT
ENST00000350908.9:c.1648-92_1648-88delinsCTGAT MANE Select	ENSP00000265436.7:n.1648-92_1648-88delins...
ENST00000393489.8:c.*1442-92_*1442-88delinsCTGAT	ENSP00000377129.4:n.*1442-92_*1442-88deli...
ENST00000350908.8:c.1648-92_1648-88delinsCTGAT	ENSP00000265436.7:n.1648-92_1648-88delins...
ENST00000393489.7:c.1372-92_1372-88delinsCTGAT	ENSP00000377129.3:n.1372-92_1372-88delins...
ENST00000393491.7:c.1093-92_1093-88delinsCTGAT	ENSP00000377130.3:n.1093-92_1093-88delins...
ENST00000393494.6:c.1648-92_1648-88delinsCTGAT	ENSP00000377132.2:n.1648-92_1648-88delins...
ENST00000393498.6:c.1585-92_1585-88delinsCTGAT	ENSP00000377135.2:n.1585-92_1585-88delins...
ENST00000403559.8:c.1699-92_1699-88delinsCTGAT	ENSP00000385069.4:n.1699-92_1699-88delins...
ENST00000408937.7:c.1723-92_1723-88delinsCTGAT	ENSP00000386200.3:n.1723-92_1723-88delins...
ENST00000412402.5:c.*1366-92_*1366-88delinsCTGAT	ENSP00000405470.1:n.*1366-92_*1366-88deli...
ENST00000441290.6:c.*1648-92_*1648-88delinsCTGAT	ENSP00000416825.1:n.*1648-92_*1648-88deli...
ENST00000634411.1:c.1597-92_1597-88delinsCTGAT	ENSP00000489135.1:n.1597-92_1597-88delins...
ENST00000634623.1:c.1588-92_1588-88delinsCTGAT	ENSP00000488944.1:n.1588-92_1588-88delins...
ENST00000634664.1:n.122+60_122+64delinsCTGAT
ENST00000635109.1:c.*1445-92_*1445-88delinsCTGAT	ENSP00000489457.1:n.*1445-92_*1445-88deli...
ENST00000635534.1:c.1639-92_1639-88delinsCTGAT	ENSP00000489229.1:n.1639-92_1639-88delins...
ENST00000635638.1:c.1651-92_1651-88delinsCTGAT	ENSP00000489073.1:n.1651-92_1651-88delins...
NM_001172766.2:c.1645-92_1645-88delinsCTGAT	NP_001166237.1:n.1645-92_1645-88delinsCTG...
NM_014491.3:c.1648-92_1648-88delinsCTGAT	NP_055306.1:n.1648-92_1648-88delinsCTGAT
NM_148898.3:c.1723-92_1723-88delinsCTGAT	NP_683696.2:n.1723-92_1723-88delinsCTGAT
NM_148900.3:c.1699-92_1699-88delinsCTGAT	NP_683698.2:n.1699-92_1699-88delinsCTGAT
NR_033766.1:n.2033-92_2033-88delinsCTGAT
NR_033767.1:n.2080-92_2080-88delinsCTGAT
XM_011516706.1:c.1792-92_1792-88delinsCTGAT	XP_011515008.1:n.1792-92_1792-88delinsCTG...
XM_017012801.2:c.1723-92_1723-88delinsCTGAT	XP_016868290.1:n.1723-92_1723-88delinsCTG...
NM_014491.4:c.1648-92_1648-88delinsCTGAT MANE Select	NP_055306.1:n.1648-92_1648-88delinsCTGAT
NM_001172766.3:c.1645-92_1645-88delinsCTGAT	NP_001166237.1:n.1645-92_1645-88delinsCTG...
NM_148898.4:c.1723-92_1723-88delinsCTGAT	NP_683696.2:n.1723-92_1723-88delinsCTGAT
NR_033766.2:n.2016-92_2016-88delinsCTGAT
NR_033767.2:n.2262-92_2262-88delinsCTGAT
NM_148900.4:c.1699-92_1699-88delinsCTGAT	NP_683698.2:n.1699-92_1699-88delinsCTGAT