Canonical Allele Identifier: CA2684564064

Gene: FOXP2

Linked Data

• gnomAD v4: 7-114661977-TTAAGTAAGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114661979_114661987del , CM000669.2:g.114661979_114661987del	GRCh38
NC_000007.13:g.114302034_114302042del , CM000669.1:g.114302034_114302042del	GRCh37
NC_000007.12:g.114089270_114089278del	NCBI36
NG_007491.2:g.580670_580678del
NG_007491.3:g.580670_580678del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1699-86_1699-78del	ENSP00000385069.4:n.1699-86_1699-78del
ENST00000703612.1:c.1639-86_1639-78del	ENSP00000515396.1:n.1639-86_1639-78del
ENST00000703613.1:c.1699-86_1699-78del	ENSP00000515397.1:n.1699-86_1699-78del
ENST00000703614.1:c.1648-86_1648-78del	ENSP00000515398.1:n.1648-86_1648-78del
ENST00000703616.1:c.1774-86_1774-78del	ENSP00000515400.1:n.1774-86_1774-78del
ENST00000703617.1:c.1093-86_1093-78del	ENSP00000515401.1:n.1093-86_1093-78del
ENST00000703618.1:c.545-86_545-78del
ENST00000350908.9:c.1648-86_1648-78del MANE Select	ENSP00000265436.7:n.1648-86_1648-78del
ENST00000393489.8:c.*1442-86_*1442-78del	ENSP00000377129.4:n.*1442-86_*1442-78del
ENST00000350908.8:c.1648-86_1648-78del	ENSP00000265436.7:n.1648-86_1648-78del
ENST00000393489.7:c.1372-86_1372-78del	ENSP00000377129.3:n.1372-86_1372-78del
ENST00000393491.7:c.1093-86_1093-78del	ENSP00000377130.3:n.1093-86_1093-78del
ENST00000393494.6:c.1648-86_1648-78del	ENSP00000377132.2:n.1648-86_1648-78del
ENST00000393498.6:c.1585-86_1585-78del	ENSP00000377135.2:n.1585-86_1585-78del
ENST00000403559.8:c.1699-86_1699-78del	ENSP00000385069.4:n.1699-86_1699-78del
ENST00000408937.7:c.1723-86_1723-78del	ENSP00000386200.3:n.1723-86_1723-78del
ENST00000412402.5:c.*1366-86_*1366-78del	ENSP00000405470.1:n.*1366-86_*1366-78del
ENST00000441290.6:c.*1648-86_*1648-78del	ENSP00000416825.1:n.*1648-86_*1648-78del
ENST00000634411.1:c.1597-86_1597-78del	ENSP00000489135.1:n.1597-86_1597-78del
ENST00000634623.1:c.1588-86_1588-78del	ENSP00000488944.1:n.1588-86_1588-78del
ENST00000634664.1:n.122+66_122+74del
ENST00000635109.1:c.*1445-86_*1445-78del	ENSP00000489457.1:n.*1445-86_*1445-78del
ENST00000635534.1:c.1639-86_1639-78del	ENSP00000489229.1:n.1639-86_1639-78del
ENST00000635638.1:c.1651-86_1651-78del	ENSP00000489073.1:n.1651-86_1651-78del
NM_001172766.2:c.1645-86_1645-78del	NP_001166237.1:n.1645-86_1645-78del
NM_014491.3:c.1648-86_1648-78del	NP_055306.1:n.1648-86_1648-78del
NM_148898.3:c.1723-86_1723-78del	NP_683696.2:n.1723-86_1723-78del
NM_148900.3:c.1699-86_1699-78del	NP_683698.2:n.1699-86_1699-78del
NR_033766.1:n.2033-86_2033-78del
NR_033767.1:n.2080-86_2080-78del
XM_011516706.1:c.1792-86_1792-78del	XP_011515008.1:n.1792-86_1792-78del
XM_017012801.2:c.1723-86_1723-78del	XP_016868290.1:n.1723-86_1723-78del
NM_014491.4:c.1648-86_1648-78del MANE Select	NP_055306.1:n.1648-86_1648-78del
NM_001172766.3:c.1645-86_1645-78del	NP_001166237.1:n.1645-86_1645-78del
NM_148898.4:c.1723-86_1723-78del	NP_683696.2:n.1723-86_1723-78del
NR_033766.2:n.2016-86_2016-78del
NR_033767.2:n.2262-86_2262-78del
NM_148900.4:c.1699-86_1699-78del	NP_683698.2:n.1699-86_1699-78del