Canonical Allele Identifier: CA2684564141
Gene: FOXP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.114662307_114662308insAAATAATATTG , CM000669.2:g.114662307_114662308insAAATAATATTG GRCh38
NC_000007.13:g.114302362_114302363insAAATAATATTG , CM000669.1:g.114302362_114302363insAAATAATATTG GRCh37
NC_000007.12:g.114089598_114089599insAAATAATATTG NCBI36
NG_007491.2:g.580998_580999insAAATAATATTG
NG_007491.3:g.580998_580999insAAATAATATTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000403559.9:c.1820+121_1820+122insAAATAATATTG ENSP00000385069.4:n.1820+121_1820+122insAAATAATATTG
ENST00000703612.1:c.1760+121_1760+122insAAATAATATTG ENSP00000515396.1:n.1760+121_1760+122insAAATAATATTG
ENST00000703613.1:c.1820+121_1820+122insAAATAATATTG ENSP00000515397.1:n.1820+121_1820+122insAAATAATATTG
ENST00000703614.1:c.1769+121_1769+122insAAATAATATTG ENSP00000515398.1:n.1769+121_1769+122insAAATAATATTG
ENST00000703616.1:c.1895+121_1895+122insAAATAATATTG ENSP00000515400.1:n.1895+121_1895+122insAAATAATATTG
ENST00000703617.1:c.1214+121_1214+122insAAATAATATTG ENSP00000515401.1:n.1214+121_1214+122insAAATAATATTG
ENST00000703618.1:c.666+121_666+122insAAATAATATTG
ENST00000350908.9:c.1769+121_1769+122insAAATAATATTG MANE Select ENSP00000265436.7:n.1769+121_1769+122insAAATAATATTG
ENST00000393489.8:c.*1563+121_*1563+122insAAATAATATTG ENSP00000377129.4:n.*1563+121_*1563+122insAAATAATATTG
ENST00000350908.8:c.1769+121_1769+122insAAATAATATTG ENSP00000265436.7:n.1769+121_1769+122insAAATAATATTG
ENST00000393489.7:c.1493+121_1493+122insAAATAATATTG ENSP00000377129.3:n.1493+121_1493+122insAAATAATATTG
ENST00000393491.7:c.1214+121_1214+122insAAATAATATTG ENSP00000377130.3:n.1214+121_1214+122insAAATAATATTG
ENST00000393494.6:c.1769+121_1769+122insAAATAATATTG ENSP00000377132.2:n.1769+121_1769+122insAAATAATATTG
ENST00000393498.6:c.1706+121_1706+122insAAATAATATTG ENSP00000377135.2:n.1706+121_1706+122insAAATAATATTG
ENST00000403559.8:c.1820+121_1820+122insAAATAATATTG ENSP00000385069.4:n.1820+121_1820+122insAAATAATATTG
ENST00000408937.7:c.1844+121_1844+122insAAATAATATTG ENSP00000386200.3:n.1844+121_1844+122insAAATAATATTG
ENST00000412402.5:c.*1487+121_*1487+122insAAATAATATTG ENSP00000405470.1:n.*1487+121_*1487+122insAAATAATATTG
ENST00000441290.6:c.*1769+121_*1769+122insAAATAATATTG ENSP00000416825.1:n.*1769+121_*1769+122insAAATAATATTG
ENST00000634411.1:c.1718+121_1718+122insAAATAATATTG ENSP00000489135.1:n.1718+121_1718+122insAAATAATATTG
ENST00000634623.1:c.1709+121_1709+122insAAATAATATTG ENSP00000488944.1:n.1709+121_1709+122insAAATAATATTG
ENST00000634664.1:n.244+121_244+122insAAATAATATTG
ENST00000635109.1:c.*1566+121_*1566+122insAAATAATATTG ENSP00000489457.1:n.*1566+121_*1566+122insAAATAATATTG
ENST00000635534.1:c.1760+121_1760+122insAAATAATATTG ENSP00000489229.1:n.1760+121_1760+122insAAATAATATTG
ENST00000635638.1:c.1772+121_1772+122insAAATAATATTG ENSP00000489073.1:n.1772+121_1772+122insAAATAATATTG
NM_001172766.2:c.1766+121_1766+122insAAATAATATTG NP_001166237.1:n.1766+121_1766+122insAAATAATATTG
NM_014491.3:c.1769+121_1769+122insAAATAATATTG NP_055306.1:n.1769+121_1769+122insAAATAATATTG
NM_148898.3:c.1844+121_1844+122insAAATAATATTG NP_683696.2:n.1844+121_1844+122insAAATAATATTG
NM_148900.3:c.1820+121_1820+122insAAATAATATTG NP_683698.2:n.1820+121_1820+122insAAATAATATTG
NR_033766.1:n.2154+121_2154+122insAAATAATATTG
NR_033767.1:n.2201+121_2201+122insAAATAATATTG
XM_011516706.1:c.1913+121_1913+122insAAATAATATTG XP_011515008.1:n.1913+121_1913+122insAAATAATATTG
XM_017012801.2:c.1844+121_1844+122insAAATAATATTG XP_016868290.1:n.1844+121_1844+122insAAATAATATTG
NM_014491.4:c.1769+121_1769+122insAAATAATATTG MANE Select NP_055306.1:n.1769+121_1769+122insAAATAATATTG
NM_001172766.3:c.1766+121_1766+122insAAATAATATTG NP_001166237.1:n.1766+121_1766+122insAAATAATATTG
NM_148898.4:c.1844+121_1844+122insAAATAATATTG NP_683696.2:n.1844+121_1844+122insAAATAATATTG
NR_033766.2:n.2137+121_2137+122insAAATAATATTG
NR_033767.2:n.2383+121_2383+122insAAATAATATTG
NM_148900.4:c.1820+121_1820+122insAAATAATATTG NP_683698.2:n.1820+121_1820+122insAAATAATATTG