Canonical Allele Identifier: CA1736047991

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662423_114662424delinsTC , CM000669.2:g.114662423_114662424delinsTC	GRCh38
NC_000007.13:g.114302478_114302479delinsTC , CM000669.1:g.114302478_114302479delinsTC	GRCh37
NC_000007.12:g.114089714_114089715delinsTC	NCBI36
NG_007491.2:g.581114_581115delinsTC
NG_007491.3:g.581114_581115delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1820+237_1820+238delinsTC	ENSP00000385069.4:n.1820+237_1820+238delinsTC
ENST00000703612.1:c.1760+237_1760+238delinsTC	ENSP00000515396.1:n.1760+237_1760+238delinsTC
ENST00000703613.1:c.1820+237_1820+238delinsTC	ENSP00000515397.1:n.1820+237_1820+238delinsTC
ENST00000703614.1:c.1769+237_1769+238delinsTC	ENSP00000515398.1:n.1769+237_1769+238delinsTC
ENST00000703616.1:c.1895+237_1895+238delinsTC	ENSP00000515400.1:n.1895+237_1895+238delinsTC
ENST00000703617.1:c.1214+237_1214+238delinsTC	ENSP00000515401.1:n.1214+237_1214+238delinsTC
ENST00000703618.1:c.666+237_666+238delinsTC
ENST00000350908.9:c.1769+237_1769+238delinsTC MANE Select	ENSP00000265436.7:n.1769+237_1769+238delinsTC
ENST00000393489.8:c.*1563+237_*1563+238delinsTC	ENSP00000377129.4:n.*1563+237_*1563+238delinsTC
ENST00000350908.8:c.1769+237_1769+238delinsTC	ENSP00000265436.7:n.1769+237_1769+238delinsTC
ENST00000393489.7:c.1493+237_1493+238delinsTC	ENSP00000377129.3:n.1493+237_1493+238delinsTC
ENST00000393491.7:c.1214+237_1214+238delinsTC	ENSP00000377130.3:n.1214+237_1214+238delinsTC
ENST00000393494.6:c.1769+237_1769+238delinsTC	ENSP00000377132.2:n.1769+237_1769+238delinsTC
ENST00000393498.6:c.1706+237_1706+238delinsTC	ENSP00000377135.2:n.1706+237_1706+238delinsTC
ENST00000403559.8:c.1820+237_1820+238delinsTC	ENSP00000385069.4:n.1820+237_1820+238delinsTC
ENST00000408937.7:c.1844+237_1844+238delinsTC	ENSP00000386200.3:n.1844+237_1844+238delinsTC
ENST00000412402.5:c.*1487+237_*1487+238delinsTC	ENSP00000405470.1:n.*1487+237_*1487+238delinsTC
ENST00000441290.6:c.*1769+237_*1769+238delinsTC	ENSP00000416825.1:n.*1769+237_*1769+238delinsTC
ENST00000634411.1:c.1718+237_1718+238delinsTC	ENSP00000489135.1:n.1718+237_1718+238delinsTC
ENST00000634623.1:c.1709+237_1709+238delinsTC	ENSP00000488944.1:n.1709+237_1709+238delinsTC
ENST00000634664.1:n.244+237_244+238delinsTC
ENST00000635109.1:c.*1566+237_*1566+238delinsTC	ENSP00000489457.1:n.*1566+237_*1566+238delinsTC
ENST00000635534.1:c.1760+237_1760+238delinsTC	ENSP00000489229.1:n.1760+237_1760+238delinsTC
ENST00000635638.1:c.1772+237_1772+238delinsTC	ENSP00000489073.1:n.1772+237_1772+238delinsTC
NM_001172766.2:c.1766+237_1766+238delinsTC	NP_001166237.1:n.1766+237_1766+238delinsTC
NM_014491.3:c.1769+237_1769+238delinsTC	NP_055306.1:n.1769+237_1769+238delinsTC
NM_148898.3:c.1844+237_1844+238delinsTC	NP_683696.2:n.1844+237_1844+238delinsTC
NM_148900.3:c.1820+237_1820+238delinsTC	NP_683698.2:n.1820+237_1820+238delinsTC
NR_033766.1:n.2154+237_2154+238delinsTC
NR_033767.1:n.2201+237_2201+238delinsTC
XM_011516706.1:c.1913+237_1913+238delinsTC	XP_011515008.1:n.1913+237_1913+238delinsTC
XM_017012801.2:c.1844+237_1844+238delinsTC	XP_016868290.1:n.1844+237_1844+238delinsTC
NM_014491.4:c.1769+237_1769+238delinsTC MANE Select	NP_055306.1:n.1769+237_1769+238delinsTC
NM_001172766.3:c.1766+237_1766+238delinsTC	NP_001166237.1:n.1766+237_1766+238delinsTC
NM_148898.4:c.1844+237_1844+238delinsTC	NP_683696.2:n.1844+237_1844+238delinsTC
NR_033766.2:n.2137+237_2137+238delinsTC
NR_033767.2:n.2383+237_2383+238delinsTC
NM_148900.4:c.1820+237_1820+238delinsTC	NP_683698.2:n.1820+237_1820+238delinsTC