Canonical Allele Identifier: CA831841552

Gene: FOXP2

Linked Data

• dbSNP Id: rs1241440884
• gnomAD v3: 7-114661973-CTGAT-C
• gnomAD v4: 7-114661973-CTGAT-C
• MyVariant Identifiers: chr7:g.114302029_114302032del (hg19) ; chr7:g.114661974_114661977del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114661975_114661978del , CM000669.2:g.114661975_114661978del	GRCh38
NC_000007.13:g.114302030_114302033del , CM000669.1:g.114302030_114302033del	GRCh37
NC_000007.12:g.114089266_114089269del	NCBI36
NG_007491.2:g.580666_580669del
NG_007491.3:g.580666_580669del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1699-90_1699-87del	ENSP00000385069.4:n.1699-90_1699-87del
ENST00000703612.1:c.1639-90_1639-87del	ENSP00000515396.1:n.1639-90_1639-87del
ENST00000703613.1:c.1699-90_1699-87del	ENSP00000515397.1:n.1699-90_1699-87del
ENST00000703614.1:c.1648-90_1648-87del	ENSP00000515398.1:n.1648-90_1648-87del
ENST00000703616.1:c.1774-90_1774-87del	ENSP00000515400.1:n.1774-90_1774-87del
ENST00000703617.1:c.1093-90_1093-87del	ENSP00000515401.1:n.1093-90_1093-87del
ENST00000703618.1:c.545-90_545-87del
ENST00000350908.9:c.1648-90_1648-87del MANE Select	ENSP00000265436.7:n.1648-90_1648-87del
ENST00000393489.8:c.*1442-90_*1442-87del	ENSP00000377129.4:n.*1442-90_*1442-87del
ENST00000350908.8:c.1648-90_1648-87del	ENSP00000265436.7:n.1648-90_1648-87del
ENST00000393489.7:c.1372-90_1372-87del	ENSP00000377129.3:n.1372-90_1372-87del
ENST00000393491.7:c.1093-90_1093-87del	ENSP00000377130.3:n.1093-90_1093-87del
ENST00000393494.6:c.1648-90_1648-87del	ENSP00000377132.2:n.1648-90_1648-87del
ENST00000393498.6:c.1585-90_1585-87del	ENSP00000377135.2:n.1585-90_1585-87del
ENST00000403559.8:c.1699-90_1699-87del	ENSP00000385069.4:n.1699-90_1699-87del
ENST00000408937.7:c.1723-90_1723-87del	ENSP00000386200.3:n.1723-90_1723-87del
ENST00000412402.5:c.*1366-90_*1366-87del	ENSP00000405470.1:n.*1366-90_*1366-87del
ENST00000441290.6:c.*1648-90_*1648-87del	ENSP00000416825.1:n.*1648-90_*1648-87del
ENST00000634411.1:c.1597-90_1597-87del	ENSP00000489135.1:n.1597-90_1597-87del
ENST00000634623.1:c.1588-90_1588-87del	ENSP00000488944.1:n.1588-90_1588-87del
ENST00000634664.1:n.122+62_122+65del
ENST00000635109.1:c.*1445-90_*1445-87del	ENSP00000489457.1:n.*1445-90_*1445-87del
ENST00000635534.1:c.1639-90_1639-87del	ENSP00000489229.1:n.1639-90_1639-87del
ENST00000635638.1:c.1651-90_1651-87del	ENSP00000489073.1:n.1651-90_1651-87del
NM_001172766.2:c.1645-90_1645-87del	NP_001166237.1:n.1645-90_1645-87del
NM_014491.3:c.1648-90_1648-87del	NP_055306.1:n.1648-90_1648-87del
NM_148898.3:c.1723-90_1723-87del	NP_683696.2:n.1723-90_1723-87del
NM_148900.3:c.1699-90_1699-87del	NP_683698.2:n.1699-90_1699-87del
NR_033766.1:n.2033-90_2033-87del
NR_033767.1:n.2080-90_2080-87del
XM_011516706.1:c.1792-90_1792-87del	XP_011515008.1:n.1792-90_1792-87del
XM_017012801.2:c.1723-90_1723-87del	XP_016868290.1:n.1723-90_1723-87del
NM_014491.4:c.1648-90_1648-87del MANE Select	NP_055306.1:n.1648-90_1648-87del
NM_001172766.3:c.1645-90_1645-87del	NP_001166237.1:n.1645-90_1645-87del
NM_148898.4:c.1723-90_1723-87del	NP_683696.2:n.1723-90_1723-87del
NR_033766.2:n.2016-90_2016-87del
NR_033767.2:n.2262-90_2262-87del
NM_148900.4:c.1699-90_1699-87del	NP_683698.2:n.1699-90_1699-87del