Canonical Allele Identifier: CA1736047913

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662244_114662245delinsCT , CM000669.2:g.114662244_114662245delinsCT	GRCh38
NC_000007.13:g.114302299_114302300delinsCT , CM000669.1:g.114302299_114302300delinsCT	GRCh37
NC_000007.12:g.114089535_114089536delinsCT	NCBI36
NG_007491.2:g.580935_580936delinsCT
NG_007491.3:g.580935_580936delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1820+58_1820+59delinsCT	ENSP00000385069.4:n.1820+58_1820+59delinsCT
ENST00000703612.1:c.1760+58_1760+59delinsCT	ENSP00000515396.1:n.1760+58_1760+59delinsCT
ENST00000703613.1:c.1820+58_1820+59delinsCT	ENSP00000515397.1:n.1820+58_1820+59delinsCT
ENST00000703614.1:c.1769+58_1769+59delinsCT	ENSP00000515398.1:n.1769+58_1769+59delinsCT
ENST00000703616.1:c.1895+58_1895+59delinsCT	ENSP00000515400.1:n.1895+58_1895+59delinsCT
ENST00000703617.1:c.1214+58_1214+59delinsCT	ENSP00000515401.1:n.1214+58_1214+59delinsCT
ENST00000703618.1:c.666+58_666+59delinsCT
ENST00000350908.9:c.1769+58_1769+59delinsCT MANE Select	ENSP00000265436.7:n.1769+58_1769+59delinsCT
ENST00000393489.8:c.*1563+58_*1563+59delinsCT	ENSP00000377129.4:n.*1563+58_*1563+59delinsCT
ENST00000350908.8:c.1769+58_1769+59delinsCT	ENSP00000265436.7:n.1769+58_1769+59delinsCT
ENST00000393489.7:c.1493+58_1493+59delinsCT	ENSP00000377129.3:n.1493+58_1493+59delinsCT
ENST00000393491.7:c.1214+58_1214+59delinsCT	ENSP00000377130.3:n.1214+58_1214+59delinsCT
ENST00000393494.6:c.1769+58_1769+59delinsCT	ENSP00000377132.2:n.1769+58_1769+59delinsCT
ENST00000393498.6:c.1706+58_1706+59delinsCT	ENSP00000377135.2:n.1706+58_1706+59delinsCT
ENST00000403559.8:c.1820+58_1820+59delinsCT	ENSP00000385069.4:n.1820+58_1820+59delinsCT
ENST00000408937.7:c.1844+58_1844+59delinsCT	ENSP00000386200.3:n.1844+58_1844+59delinsCT
ENST00000412402.5:c.*1487+58_*1487+59delinsCT	ENSP00000405470.1:n.*1487+58_*1487+59delinsCT
ENST00000441290.6:c.*1769+58_*1769+59delinsCT	ENSP00000416825.1:n.*1769+58_*1769+59delinsCT
ENST00000634411.1:c.1718+58_1718+59delinsCT	ENSP00000489135.1:n.1718+58_1718+59delinsCT
ENST00000634623.1:c.1709+58_1709+59delinsCT	ENSP00000488944.1:n.1709+58_1709+59delinsCT
ENST00000634664.1:n.244+58_244+59delinsCT
ENST00000635109.1:c.*1566+58_*1566+59delinsCT	ENSP00000489457.1:n.*1566+58_*1566+59delinsCT
ENST00000635534.1:c.1760+58_1760+59delinsCT	ENSP00000489229.1:n.1760+58_1760+59delinsCT
ENST00000635638.1:c.1772+58_1772+59delinsCT	ENSP00000489073.1:n.1772+58_1772+59delinsCT
NM_001172766.2:c.1766+58_1766+59delinsCT	NP_001166237.1:n.1766+58_1766+59delinsCT
NM_014491.3:c.1769+58_1769+59delinsCT	NP_055306.1:n.1769+58_1769+59delinsCT
NM_148898.3:c.1844+58_1844+59delinsCT	NP_683696.2:n.1844+58_1844+59delinsCT
NM_148900.3:c.1820+58_1820+59delinsCT	NP_683698.2:n.1820+58_1820+59delinsCT
NR_033766.1:n.2154+58_2154+59delinsCT
NR_033767.1:n.2201+58_2201+59delinsCT
XM_011516706.1:c.1913+58_1913+59delinsCT	XP_011515008.1:n.1913+58_1913+59delinsCT
XM_017012801.2:c.1844+58_1844+59delinsCT	XP_016868290.1:n.1844+58_1844+59delinsCT
NM_014491.4:c.1769+58_1769+59delinsCT MANE Select	NP_055306.1:n.1769+58_1769+59delinsCT
NM_001172766.3:c.1766+58_1766+59delinsCT	NP_001166237.1:n.1766+58_1766+59delinsCT
NM_148898.4:c.1844+58_1844+59delinsCT	NP_683696.2:n.1844+58_1844+59delinsCT
NR_033766.2:n.2137+58_2137+59delinsCT
NR_033767.2:n.2383+58_2383+59delinsCT
NM_148900.4:c.1820+58_1820+59delinsCT	NP_683698.2:n.1820+58_1820+59delinsCT