Canonical Allele Identifier: CA2684564074

Gene: FOXP2

Linked Data

• gnomAD v4: 7-114661994-TGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114661998_114662000del , CM000669.2:g.114661998_114662000del	GRCh38
NC_000007.13:g.114302053_114302055del , CM000669.1:g.114302053_114302055del	GRCh37
NC_000007.12:g.114089289_114089291del	NCBI36
NG_007491.2:g.580689_580691del
NG_007491.3:g.580689_580691del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1699-67_1699-65del	ENSP00000385069.4:n.1699-67_1699-65del
ENST00000703612.1:c.1639-67_1639-65del	ENSP00000515396.1:n.1639-67_1639-65del
ENST00000703613.1:c.1699-67_1699-65del	ENSP00000515397.1:n.1699-67_1699-65del
ENST00000703614.1:c.1648-67_1648-65del	ENSP00000515398.1:n.1648-67_1648-65del
ENST00000703616.1:c.1774-67_1774-65del	ENSP00000515400.1:n.1774-67_1774-65del
ENST00000703617.1:c.1093-67_1093-65del	ENSP00000515401.1:n.1093-67_1093-65del
ENST00000703618.1:c.545-67_545-65del
ENST00000350908.9:c.1648-67_1648-65del MANE Select	ENSP00000265436.7:n.1648-67_1648-65del
ENST00000393489.8:c.*1442-67_*1442-65del	ENSP00000377129.4:n.*1442-67_*1442-65del
ENST00000350908.8:c.1648-67_1648-65del	ENSP00000265436.7:n.1648-67_1648-65del
ENST00000393489.7:c.1372-67_1372-65del	ENSP00000377129.3:n.1372-67_1372-65del
ENST00000393491.7:c.1093-67_1093-65del	ENSP00000377130.3:n.1093-67_1093-65del
ENST00000393494.6:c.1648-67_1648-65del	ENSP00000377132.2:n.1648-67_1648-65del
ENST00000393498.6:c.1585-67_1585-65del	ENSP00000377135.2:n.1585-67_1585-65del
ENST00000403559.8:c.1699-67_1699-65del	ENSP00000385069.4:n.1699-67_1699-65del
ENST00000408937.7:c.1723-67_1723-65del	ENSP00000386200.3:n.1723-67_1723-65del
ENST00000412402.5:c.*1366-67_*1366-65del	ENSP00000405470.1:n.*1366-67_*1366-65del
ENST00000441290.6:c.*1648-67_*1648-65del	ENSP00000416825.1:n.*1648-67_*1648-65del
ENST00000634411.1:c.1597-67_1597-65del	ENSP00000489135.1:n.1597-67_1597-65del
ENST00000634623.1:c.1588-67_1588-65del	ENSP00000488944.1:n.1588-67_1588-65del
ENST00000634664.1:n.123-67_123-65del
ENST00000635109.1:c.*1445-67_*1445-65del	ENSP00000489457.1:n.*1445-67_*1445-65del
ENST00000635534.1:c.1639-67_1639-65del	ENSP00000489229.1:n.1639-67_1639-65del
ENST00000635638.1:c.1651-67_1651-65del	ENSP00000489073.1:n.1651-67_1651-65del
NM_001172766.2:c.1645-67_1645-65del	NP_001166237.1:n.1645-67_1645-65del
NM_014491.3:c.1648-67_1648-65del	NP_055306.1:n.1648-67_1648-65del
NM_148898.3:c.1723-67_1723-65del	NP_683696.2:n.1723-67_1723-65del
NM_148900.3:c.1699-67_1699-65del	NP_683698.2:n.1699-67_1699-65del
NR_033766.1:n.2033-67_2033-65del
NR_033767.1:n.2080-67_2080-65del
XM_011516706.1:c.1792-67_1792-65del	XP_011515008.1:n.1792-67_1792-65del
XM_017012801.2:c.1723-67_1723-65del	XP_016868290.1:n.1723-67_1723-65del
NM_014491.4:c.1648-67_1648-65del MANE Select	NP_055306.1:n.1648-67_1648-65del
NM_001172766.3:c.1645-67_1645-65del	NP_001166237.1:n.1645-67_1645-65del
NM_148898.4:c.1723-67_1723-65del	NP_683696.2:n.1723-67_1723-65del
NR_033766.2:n.2016-67_2016-65del
NR_033767.2:n.2262-67_2262-65del
NM_148900.4:c.1699-67_1699-65del	NP_683698.2:n.1699-67_1699-65del