Canonical Allele Identifier: CA1736048018

Gene: FOXP2

Linked Data

• dbSNP Id: rs143165509

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662478_114662481del , CM000669.2:g.114662478_114662481del	GRCh38
NC_000007.13:g.114302533_114302536del , CM000669.1:g.114302533_114302536del	GRCh37
NC_000007.12:g.114089769_114089772del	NCBI36
NG_007491.2:g.581169_581172del
NG_007491.3:g.581169_581172del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1820+292_1820+295del	ENSP00000385069.4:n.1820+292_1820+295del
ENST00000703612.1:c.1760+292_1760+295del	ENSP00000515396.1:n.1760+292_1760+295del
ENST00000703613.1:c.1820+292_1820+295del	ENSP00000515397.1:n.1820+292_1820+295del
ENST00000703614.1:c.1769+292_1769+295del	ENSP00000515398.1:n.1769+292_1769+295del
ENST00000703616.1:c.1895+292_1895+295del	ENSP00000515400.1:n.1895+292_1895+295del
ENST00000703617.1:c.1214+292_1214+295del	ENSP00000515401.1:n.1214+292_1214+295del
ENST00000703618.1:c.666+292_666+295del
ENST00000350908.9:c.1769+292_1769+295del MANE Select	ENSP00000265436.7:n.1769+292_1769+295del
ENST00000393489.8:c.*1563+292_*1563+295del	ENSP00000377129.4:n.*1563+292_*1563+295del
ENST00000350908.8:c.1769+292_1769+295del	ENSP00000265436.7:n.1769+292_1769+295del
ENST00000393489.7:c.1493+292_1493+295del	ENSP00000377129.3:n.1493+292_1493+295del
ENST00000393491.7:c.1214+292_1214+295del	ENSP00000377130.3:n.1214+292_1214+295del
ENST00000393494.6:c.1769+292_1769+295del	ENSP00000377132.2:n.1769+292_1769+295del
ENST00000393498.6:c.1706+292_1706+295del	ENSP00000377135.2:n.1706+292_1706+295del
ENST00000403559.8:c.1820+292_1820+295del	ENSP00000385069.4:n.1820+292_1820+295del
ENST00000408937.7:c.1844+292_1844+295del	ENSP00000386200.3:n.1844+292_1844+295del
ENST00000412402.5:c.*1487+292_*1487+295del	ENSP00000405470.1:n.*1487+292_*1487+295del
ENST00000441290.6:c.*1769+292_*1769+295del	ENSP00000416825.1:n.*1769+292_*1769+295del
ENST00000634411.1:c.1718+292_1718+295del	ENSP00000489135.1:n.1718+292_1718+295del
ENST00000634623.1:c.1709+292_1709+295del	ENSP00000488944.1:n.1709+292_1709+295del
ENST00000634664.1:n.244+292_244+295del
ENST00000635109.1:c.*1566+292_*1566+295del	ENSP00000489457.1:n.*1566+292_*1566+295del
ENST00000635534.1:c.1760+292_1760+295del	ENSP00000489229.1:n.1760+292_1760+295del
ENST00000635638.1:c.1772+292_1772+295del	ENSP00000489073.1:n.1772+292_1772+295del
NM_001172766.2:c.1766+292_1766+295del	NP_001166237.1:n.1766+292_1766+295del
NM_014491.3:c.1769+292_1769+295del	NP_055306.1:n.1769+292_1769+295del
NM_148898.3:c.1844+292_1844+295del	NP_683696.2:n.1844+292_1844+295del
NM_148900.3:c.1820+292_1820+295del	NP_683698.2:n.1820+292_1820+295del
NR_033766.1:n.2154+292_2154+295del
NR_033767.1:n.2201+292_2201+295del
XM_011516706.1:c.1913+292_1913+295del	XP_011515008.1:n.1913+292_1913+295del
XM_017012801.2:c.1844+292_1844+295del	XP_016868290.1:n.1844+292_1844+295del
NM_014491.4:c.1769+292_1769+295del MANE Select	NP_055306.1:n.1769+292_1769+295del
NM_001172766.3:c.1766+292_1766+295del	NP_001166237.1:n.1766+292_1766+295del
NM_148898.4:c.1844+292_1844+295del	NP_683696.2:n.1844+292_1844+295del
NR_033766.2:n.2137+292_2137+295del
NR_033767.2:n.2383+292_2383+295del
NM_148900.4:c.1820+292_1820+295del	NP_683698.2:n.1820+292_1820+295del