Canonical Allele Identifier: CA577216395

Gene: FOXP2

Linked Data

• dbSNP Id: rs1391366696
• gnomAD v2: 7-114302326-CAGTT-C
• gnomAD v3: 7-114662271-CAGTT-C
• gnomAD v4: 7-114662271-CAGTT-C
• MyVariant Identifiers: chr7:g.114302327_114302330del (hg19) ; chr7:g.114662272_114662275del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662274_114662277del , CM000669.2:g.114662274_114662277del	GRCh38
NC_000007.13:g.114302329_114302332del , CM000669.1:g.114302329_114302332del	GRCh37
NC_000007.12:g.114089565_114089568del	NCBI36
NG_007491.2:g.580965_580968del
NG_007491.3:g.580965_580968del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1820+88_1820+91del	ENSP00000385069.4:n.1820+88_1820+91del
ENST00000703612.1:c.1760+88_1760+91del	ENSP00000515396.1:n.1760+88_1760+91del
ENST00000703613.1:c.1820+88_1820+91del	ENSP00000515397.1:n.1820+88_1820+91del
ENST00000703614.1:c.1769+88_1769+91del	ENSP00000515398.1:n.1769+88_1769+91del
ENST00000703616.1:c.1895+88_1895+91del	ENSP00000515400.1:n.1895+88_1895+91del
ENST00000703617.1:c.1214+88_1214+91del	ENSP00000515401.1:n.1214+88_1214+91del
ENST00000703618.1:c.666+88_666+91del
ENST00000350908.9:c.1769+88_1769+91del MANE Select	ENSP00000265436.7:n.1769+88_1769+91del
ENST00000393489.8:c.*1563+88_*1563+91del	ENSP00000377129.4:n.*1563+88_*1563+91del
ENST00000350908.8:c.1769+88_1769+91del	ENSP00000265436.7:n.1769+88_1769+91del
ENST00000393489.7:c.1493+88_1493+91del	ENSP00000377129.3:n.1493+88_1493+91del
ENST00000393491.7:c.1214+88_1214+91del	ENSP00000377130.3:n.1214+88_1214+91del
ENST00000393494.6:c.1769+88_1769+91del	ENSP00000377132.2:n.1769+88_1769+91del
ENST00000393498.6:c.1706+88_1706+91del	ENSP00000377135.2:n.1706+88_1706+91del
ENST00000403559.8:c.1820+88_1820+91del	ENSP00000385069.4:n.1820+88_1820+91del
ENST00000408937.7:c.1844+88_1844+91del	ENSP00000386200.3:n.1844+88_1844+91del
ENST00000412402.5:c.*1487+88_*1487+91del	ENSP00000405470.1:n.*1487+88_*1487+91del
ENST00000441290.6:c.*1769+88_*1769+91del	ENSP00000416825.1:n.*1769+88_*1769+91del
ENST00000634411.1:c.1718+88_1718+91del	ENSP00000489135.1:n.1718+88_1718+91del
ENST00000634623.1:c.1709+88_1709+91del	ENSP00000488944.1:n.1709+88_1709+91del
ENST00000634664.1:n.244+88_244+91del
ENST00000635109.1:c.*1566+88_*1566+91del	ENSP00000489457.1:n.*1566+88_*1566+91del
ENST00000635534.1:c.1760+88_1760+91del	ENSP00000489229.1:n.1760+88_1760+91del
ENST00000635638.1:c.1772+88_1772+91del	ENSP00000489073.1:n.1772+88_1772+91del
NM_001172766.2:c.1766+88_1766+91del	NP_001166237.1:n.1766+88_1766+91del
NM_014491.3:c.1769+88_1769+91del	NP_055306.1:n.1769+88_1769+91del
NM_148898.3:c.1844+88_1844+91del	NP_683696.2:n.1844+88_1844+91del
NM_148900.3:c.1820+88_1820+91del	NP_683698.2:n.1820+88_1820+91del
NR_033766.1:n.2154+88_2154+91del
NR_033767.1:n.2201+88_2201+91del
XM_011516706.1:c.1913+88_1913+91del	XP_011515008.1:n.1913+88_1913+91del
XM_017012801.2:c.1844+88_1844+91del	XP_016868290.1:n.1844+88_1844+91del
NM_014491.4:c.1769+88_1769+91del MANE Select	NP_055306.1:n.1769+88_1769+91del
NM_001172766.3:c.1766+88_1766+91del	NP_001166237.1:n.1766+88_1766+91del
NM_148898.4:c.1844+88_1844+91del	NP_683696.2:n.1844+88_1844+91del
NR_033766.2:n.2137+88_2137+91del
NR_033767.2:n.2383+88_2383+91del
NM_148900.4:c.1820+88_1820+91del	NP_683698.2:n.1820+88_1820+91del