Canonical Allele Identifier: CA1736047811

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114661977_114661981delinsTTAAG , CM000669.2:g.114661977_114661981delinsTTAAG	GRCh38
NC_000007.13:g.114302032_114302036delinsTTAAG , CM000669.1:g.114302032_114302036delinsTTAAG	GRCh37
NC_000007.12:g.114089268_114089272delinsTTAAG	NCBI36
NG_007491.2:g.580668_580672delinsTTAAG
NG_007491.3:g.580668_580672delinsTTAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1699-88_1699-84delinsTTAAG	ENSP00000385069.4:n.1699-88_1699-84delins...
ENST00000703612.1:c.1639-88_1639-84delinsTTAAG	ENSP00000515396.1:n.1639-88_1639-84delins...
ENST00000703613.1:c.1699-88_1699-84delinsTTAAG	ENSP00000515397.1:n.1699-88_1699-84delins...
ENST00000703614.1:c.1648-88_1648-84delinsTTAAG	ENSP00000515398.1:n.1648-88_1648-84delins...
ENST00000703616.1:c.1774-88_1774-84delinsTTAAG	ENSP00000515400.1:n.1774-88_1774-84delins...
ENST00000703617.1:c.1093-88_1093-84delinsTTAAG	ENSP00000515401.1:n.1093-88_1093-84delins...
ENST00000703618.1:c.545-88_545-84delinsTTAAG
ENST00000350908.9:c.1648-88_1648-84delinsTTAAG MANE Select	ENSP00000265436.7:n.1648-88_1648-84delins...
ENST00000393489.8:c.*1442-88_*1442-84delinsTTAAG	ENSP00000377129.4:n.*1442-88_*1442-84deli...
ENST00000350908.8:c.1648-88_1648-84delinsTTAAG	ENSP00000265436.7:n.1648-88_1648-84delins...
ENST00000393489.7:c.1372-88_1372-84delinsTTAAG	ENSP00000377129.3:n.1372-88_1372-84delins...
ENST00000393491.7:c.1093-88_1093-84delinsTTAAG	ENSP00000377130.3:n.1093-88_1093-84delins...
ENST00000393494.6:c.1648-88_1648-84delinsTTAAG	ENSP00000377132.2:n.1648-88_1648-84delins...
ENST00000393498.6:c.1585-88_1585-84delinsTTAAG	ENSP00000377135.2:n.1585-88_1585-84delins...
ENST00000403559.8:c.1699-88_1699-84delinsTTAAG	ENSP00000385069.4:n.1699-88_1699-84delins...
ENST00000408937.7:c.1723-88_1723-84delinsTTAAG	ENSP00000386200.3:n.1723-88_1723-84delins...
ENST00000412402.5:c.*1366-88_*1366-84delinsTTAAG	ENSP00000405470.1:n.*1366-88_*1366-84deli...
ENST00000441290.6:c.*1648-88_*1648-84delinsTTAAG	ENSP00000416825.1:n.*1648-88_*1648-84deli...
ENST00000634411.1:c.1597-88_1597-84delinsTTAAG	ENSP00000489135.1:n.1597-88_1597-84delins...
ENST00000634623.1:c.1588-88_1588-84delinsTTAAG	ENSP00000488944.1:n.1588-88_1588-84delins...
ENST00000634664.1:n.122+64_122+68delinsTTAAG
ENST00000635109.1:c.*1445-88_*1445-84delinsTTAAG	ENSP00000489457.1:n.*1445-88_*1445-84deli...
ENST00000635534.1:c.1639-88_1639-84delinsTTAAG	ENSP00000489229.1:n.1639-88_1639-84delins...
ENST00000635638.1:c.1651-88_1651-84delinsTTAAG	ENSP00000489073.1:n.1651-88_1651-84delins...
NM_001172766.2:c.1645-88_1645-84delinsTTAAG	NP_001166237.1:n.1645-88_1645-84delinsTTA...
NM_014491.3:c.1648-88_1648-84delinsTTAAG	NP_055306.1:n.1648-88_1648-84delinsTTAAG
NM_148898.3:c.1723-88_1723-84delinsTTAAG	NP_683696.2:n.1723-88_1723-84delinsTTAAG
NM_148900.3:c.1699-88_1699-84delinsTTAAG	NP_683698.2:n.1699-88_1699-84delinsTTAAG
NR_033766.1:n.2033-88_2033-84delinsTTAAG
NR_033767.1:n.2080-88_2080-84delinsTTAAG
XM_011516706.1:c.1792-88_1792-84delinsTTAAG	XP_011515008.1:n.1792-88_1792-84delinsTTA...
XM_017012801.2:c.1723-88_1723-84delinsTTAAG	XP_016868290.1:n.1723-88_1723-84delinsTTA...
NM_014491.4:c.1648-88_1648-84delinsTTAAG MANE Select	NP_055306.1:n.1648-88_1648-84delinsTTAAG
NM_001172766.3:c.1645-88_1645-84delinsTTAAG	NP_001166237.1:n.1645-88_1645-84delinsTTA...
NM_148898.4:c.1723-88_1723-84delinsTTAAG	NP_683696.2:n.1723-88_1723-84delinsTTAAG
NR_033766.2:n.2016-88_2016-84delinsTTAAG
NR_033767.2:n.2262-88_2262-84delinsTTAAG
NM_148900.4:c.1699-88_1699-84delinsTTAAG	NP_683698.2:n.1699-88_1699-84delinsTTAAG