Canonical Allele Identifier: CA1736048025
Gene: FOXP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.114662487_114662509delinsCCTGTTTTTATACAATACAGTAG , CM000669.2:g.114662487_114662509delinsCCTGTTTTTATACAATACAGTAG GRCh38
NC_000007.13:g.114302542_114302564delinsCCTGTTTTTATACAATACAGTAG , CM000669.1:g.114302542_114302564delinsCCTGTTTTTATACAATACAGTAG GRCh37
NC_000007.12:g.114089778_114089800delinsCCTGTTTTTATACAATACAGTAG NCBI36
NG_007491.2:g.581178_581200delinsCCTGTTTTTATACAATACAGTAG
NG_007491.3:g.581178_581200delinsCCTGTTTTTATACAATACAGTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000403559.9:c.1820+301_1820+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000385069.4:n.1820+301_1820+323delinsCCTGTTTTTATACAATAC...
ENST00000703612.1:c.1760+301_1760+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000515396.1:n.1760+301_1760+323delinsCCTGTTTTTATACAATAC...
ENST00000703613.1:c.1820+301_1820+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000515397.1:n.1820+301_1820+323delinsCCTGTTTTTATACAATAC...
ENST00000703614.1:c.1769+301_1769+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000515398.1:n.1769+301_1769+323delinsCCTGTTTTTATACAATAC...
ENST00000703616.1:c.1895+301_1895+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000515400.1:n.1895+301_1895+323delinsCCTGTTTTTATACAATAC...
ENST00000703617.1:c.1214+301_1214+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000515401.1:n.1214+301_1214+323delinsCCTGTTTTTATACAATAC...
ENST00000703618.1:c.666+301_666+323delinsCCTGTTTTTATACAATACAGTAG
ENST00000350908.9:c.1769+301_1769+323delinsCCTGTTTTTATACAATACAGTAG MANE Select ENSP00000265436.7:n.1769+301_1769+323delinsCCTGTTTTTATACAATAC...
ENST00000393489.8:c.*1563+301_*1563+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000377129.4:n.*1563+301_*1563+323delinsCCTGTTTTTATACAAT...
ENST00000350908.8:c.1769+301_1769+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000265436.7:n.1769+301_1769+323delinsCCTGTTTTTATACAATAC...
ENST00000393489.7:c.1493+301_1493+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000377129.3:n.1493+301_1493+323delinsCCTGTTTTTATACAATAC...
ENST00000393491.7:c.1214+301_1214+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000377130.3:n.1214+301_1214+323delinsCCTGTTTTTATACAATAC...
ENST00000393494.6:c.1769+301_1769+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000377132.2:n.1769+301_1769+323delinsCCTGTTTTTATACAATAC...
ENST00000393498.6:c.1706+301_1706+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000377135.2:n.1706+301_1706+323delinsCCTGTTTTTATACAATAC...
ENST00000403559.8:c.1820+301_1820+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000385069.4:n.1820+301_1820+323delinsCCTGTTTTTATACAATAC...
ENST00000408937.7:c.1844+301_1844+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000386200.3:n.1844+301_1844+323delinsCCTGTTTTTATACAATAC...
ENST00000412402.5:c.*1487+301_*1487+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000405470.1:n.*1487+301_*1487+323delinsCCTGTTTTTATACAAT...
ENST00000441290.6:c.*1769+301_*1769+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000416825.1:n.*1769+301_*1769+323delinsCCTGTTTTTATACAAT...
ENST00000634411.1:c.1718+301_1718+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000489135.1:n.1718+301_1718+323delinsCCTGTTTTTATACAATAC...
ENST00000634623.1:c.1709+301_1709+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000488944.1:n.1709+301_1709+323delinsCCTGTTTTTATACAATAC...
ENST00000634664.1:n.244+301_244+323delinsCCTGTTTTTATACAATACAGTAG
ENST00000635109.1:c.*1566+301_*1566+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000489457.1:n.*1566+301_*1566+323delinsCCTGTTTTTATACAAT...
ENST00000635534.1:c.1760+301_1760+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000489229.1:n.1760+301_1760+323delinsCCTGTTTTTATACAATAC...
ENST00000635638.1:c.1772+301_1772+323delinsCCTGTTTTTATACAATACAGTAG ENSP00000489073.1:n.1772+301_1772+323delinsCCTGTTTTTATACAATAC...
NM_001172766.2:c.1766+301_1766+323delinsCCTGTTTTTATACAATACAGTAG NP_001166237.1:n.1766+301_1766+323delinsCCTGTTTTTATACAATACAGT...
NM_014491.3:c.1769+301_1769+323delinsCCTGTTTTTATACAATACAGTAG NP_055306.1:n.1769+301_1769+323delinsCCTGTTTTTATACAATACAGTAG
NM_148898.3:c.1844+301_1844+323delinsCCTGTTTTTATACAATACAGTAG NP_683696.2:n.1844+301_1844+323delinsCCTGTTTTTATACAATACAGTAG
NM_148900.3:c.1820+301_1820+323delinsCCTGTTTTTATACAATACAGTAG NP_683698.2:n.1820+301_1820+323delinsCCTGTTTTTATACAATACAGTAG
NR_033766.1:n.2154+301_2154+323delinsCCTGTTTTTATACAATACAGTAG
NR_033767.1:n.2201+301_2201+323delinsCCTGTTTTTATACAATACAGTAG
XM_011516706.1:c.1913+301_1913+323delinsCCTGTTTTTATACAATACAGTAG XP_011515008.1:n.1913+301_1913+323delinsCCTGTTTTTATACAATACAGT...
XM_017012801.2:c.1844+301_1844+323delinsCCTGTTTTTATACAATACAGTAG XP_016868290.1:n.1844+301_1844+323delinsCCTGTTTTTATACAATACAGT...
NM_014491.4:c.1769+301_1769+323delinsCCTGTTTTTATACAATACAGTAG MANE Select NP_055306.1:n.1769+301_1769+323delinsCCTGTTTTTATACAATACAGTAG
NM_001172766.3:c.1766+301_1766+323delinsCCTGTTTTTATACAATACAGTAG NP_001166237.1:n.1766+301_1766+323delinsCCTGTTTTTATACAATACAGT...
NM_148898.4:c.1844+301_1844+323delinsCCTGTTTTTATACAATACAGTAG NP_683696.2:n.1844+301_1844+323delinsCCTGTTTTTATACAATACAGTAG
NR_033766.2:n.2137+301_2137+323delinsCCTGTTTTTATACAATACAGTAG
NR_033767.2:n.2383+301_2383+323delinsCCTGTTTTTATACAATACAGTAG
NM_148900.4:c.1820+301_1820+323delinsCCTGTTTTTATACAATACAGTAG NP_683698.2:n.1820+301_1820+323delinsCCTGTTTTTATACAATACAGTAG