Canonical Allele Identifier: CA2506108511

Gene: FOXP2

Linked Data

• gnomAD v4: 7-114659710-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659710_114659711insTT , CM000669.2:g.114659710_114659711insTT	GRCh38
NC_000007.13:g.114299765_114299766insTT , CM000669.1:g.114299765_114299766insTT	GRCh37
NC_000007.12:g.114087001_114087002insTT	NCBI36
NG_007491.2:g.578401_578402insTT
NG_007491.3:g.578401_578402insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1698+37_1698+38insTT	ENSP00000385069.4:n.1698+37_1698+38insTT
ENST00000703612.1:c.1638+37_1638+38insTT	ENSP00000515396.1:n.1638+37_1638+38insTT
ENST00000703613.1:c.1698+37_1698+38insTT	ENSP00000515397.1:n.1698+37_1698+38insTT
ENST00000703614.1:c.1647+37_1647+38insTT	ENSP00000515398.1:n.1647+37_1647+38insTT
ENST00000703616.1:c.1773+37_1773+38insTT	ENSP00000515400.1:n.1773+37_1773+38insTT
ENST00000703617.1:c.1092+37_1092+38insTT	ENSP00000515401.1:n.1092+37_1092+38insTT
ENST00000703618.1:c.545-2355_545-2354insTT
ENST00000350908.9:c.1647+37_1647+38insTT MANE Select	ENSP00000265436.7:n.1647+37_1647+38insTT
ENST00000393489.8:c.*1441+37_*1441+38insTT	ENSP00000377129.4:n.*1441+37_*1441+38insTT
ENST00000350908.8:c.1647+37_1647+38insTT	ENSP00000265436.7:n.1647+37_1647+38insTT
ENST00000393489.7:c.1371+37_1371+38insTT	ENSP00000377129.3:n.1371+37_1371+38insTT
ENST00000393491.7:c.1092+37_1092+38insTT	ENSP00000377130.3:n.1092+37_1092+38insTT
ENST00000393494.6:c.1647+37_1647+38insTT	ENSP00000377132.2:n.1647+37_1647+38insTT
ENST00000393498.6:c.1584+37_1584+38insTT	ENSP00000377135.2:n.1584+37_1584+38insTT
ENST00000403559.8:c.1698+37_1698+38insTT	ENSP00000385069.4:n.1698+37_1698+38insTT
ENST00000408937.7:c.1722+37_1722+38insTT	ENSP00000386200.3:n.1722+37_1722+38insTT
ENST00000412402.5:c.*1365+37_*1365+38insTT	ENSP00000405470.1:n.*1365+37_*1365+38insTT
ENST00000441290.6:c.*1647+37_*1647+38insTT	ENSP00000416825.1:n.*1647+37_*1647+38insTT
ENST00000634411.1:c.1596+37_1596+38insTT	ENSP00000489135.1:n.1596+37_1596+38insTT
ENST00000634623.1:c.1587+37_1587+38insTT	ENSP00000488944.1:n.1587+37_1587+38insTT
ENST00000635109.1:c.*1444+37_*1444+38insTT	ENSP00000489457.1:n.*1444+37_*1444+38insTT
ENST00000635534.1:c.1638+37_1638+38insTT	ENSP00000489229.1:n.1638+37_1638+38insTT
ENST00000635638.1:c.1650+37_1650+38insTT	ENSP00000489073.1:n.1650+37_1650+38insTT
NM_001172766.2:c.1644+37_1644+38insTT	NP_001166237.1:n.1644+37_1644+38insTT
NM_014491.3:c.1647+37_1647+38insTT	NP_055306.1:n.1647+37_1647+38insTT
NM_148898.3:c.1722+37_1722+38insTT	NP_683696.2:n.1722+37_1722+38insTT
NM_148900.3:c.1698+37_1698+38insTT	NP_683698.2:n.1698+37_1698+38insTT
NR_033766.1:n.2032+37_2032+38insTT
NR_033767.1:n.2079+37_2079+38insTT
XM_011516706.1:c.1791+37_1791+38insTT	XP_011515008.1:n.1791+37_1791+38insTT
XM_017012801.2:c.1722+37_1722+38insTT	XP_016868290.1:n.1722+37_1722+38insTT
NM_014491.4:c.1647+37_1647+38insTT MANE Select	NP_055306.1:n.1647+37_1647+38insTT
NM_001172766.3:c.1644+37_1644+38insTT	NP_001166237.1:n.1644+37_1644+38insTT
NM_148898.4:c.1722+37_1722+38insTT	NP_683696.2:n.1722+37_1722+38insTT
NR_033766.2:n.2015+37_2015+38insTT
NR_033767.2:n.2261+37_2261+38insTT
NM_148900.4:c.1698+37_1698+38insTT	NP_683698.2:n.1698+37_1698+38insTT