Canonical Allele Identifier: CA1736047910

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662241_114662246delinsATACTT , CM000669.2:g.114662241_114662246delinsATACTT	GRCh38
NC_000007.13:g.114302296_114302301delinsATACTT , CM000669.1:g.114302296_114302301delinsATACTT	GRCh37
NC_000007.12:g.114089532_114089537delinsATACTT	NCBI36
NG_007491.2:g.580932_580937delinsATACTT
NG_007491.3:g.580932_580937delinsATACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1820+55_1820+60delinsATACTT	ENSP00000385069.4:n.1820+55_1820+60delinsATACTT
ENST00000703612.1:c.1760+55_1760+60delinsATACTT	ENSP00000515396.1:n.1760+55_1760+60delinsATACTT
ENST00000703613.1:c.1820+55_1820+60delinsATACTT	ENSP00000515397.1:n.1820+55_1820+60delinsATACTT
ENST00000703614.1:c.1769+55_1769+60delinsATACTT	ENSP00000515398.1:n.1769+55_1769+60delinsATACTT
ENST00000703616.1:c.1895+55_1895+60delinsATACTT	ENSP00000515400.1:n.1895+55_1895+60delinsATACTT
ENST00000703617.1:c.1214+55_1214+60delinsATACTT	ENSP00000515401.1:n.1214+55_1214+60delinsATACTT
ENST00000703618.1:c.666+55_666+60delinsATACTT
ENST00000350908.9:c.1769+55_1769+60delinsATACTT MANE Select	ENSP00000265436.7:n.1769+55_1769+60delinsATACTT
ENST00000393489.8:c.*1563+55_*1563+60delinsATACTT	ENSP00000377129.4:n.*1563+55_*1563+60delinsATACTT
ENST00000350908.8:c.1769+55_1769+60delinsATACTT	ENSP00000265436.7:n.1769+55_1769+60delinsATACTT
ENST00000393489.7:c.1493+55_1493+60delinsATACTT	ENSP00000377129.3:n.1493+55_1493+60delinsATACTT
ENST00000393491.7:c.1214+55_1214+60delinsATACTT	ENSP00000377130.3:n.1214+55_1214+60delinsATACTT
ENST00000393494.6:c.1769+55_1769+60delinsATACTT	ENSP00000377132.2:n.1769+55_1769+60delinsATACTT
ENST00000393498.6:c.1706+55_1706+60delinsATACTT	ENSP00000377135.2:n.1706+55_1706+60delinsATACTT
ENST00000403559.8:c.1820+55_1820+60delinsATACTT	ENSP00000385069.4:n.1820+55_1820+60delinsATACTT
ENST00000408937.7:c.1844+55_1844+60delinsATACTT	ENSP00000386200.3:n.1844+55_1844+60delinsATACTT
ENST00000412402.5:c.*1487+55_*1487+60delinsATACTT	ENSP00000405470.1:n.*1487+55_*1487+60delinsATACTT
ENST00000441290.6:c.*1769+55_*1769+60delinsATACTT	ENSP00000416825.1:n.*1769+55_*1769+60delinsATACTT
ENST00000634411.1:c.1718+55_1718+60delinsATACTT	ENSP00000489135.1:n.1718+55_1718+60delinsATACTT
ENST00000634623.1:c.1709+55_1709+60delinsATACTT	ENSP00000488944.1:n.1709+55_1709+60delinsATACTT
ENST00000634664.1:n.244+55_244+60delinsATACTT
ENST00000635109.1:c.*1566+55_*1566+60delinsATACTT	ENSP00000489457.1:n.*1566+55_*1566+60delinsATACTT
ENST00000635534.1:c.1760+55_1760+60delinsATACTT	ENSP00000489229.1:n.1760+55_1760+60delinsATACTT
ENST00000635638.1:c.1772+55_1772+60delinsATACTT	ENSP00000489073.1:n.1772+55_1772+60delinsATACTT
NM_001172766.2:c.1766+55_1766+60delinsATACTT	NP_001166237.1:n.1766+55_1766+60delinsATACTT
NM_014491.3:c.1769+55_1769+60delinsATACTT	NP_055306.1:n.1769+55_1769+60delinsATACTT
NM_148898.3:c.1844+55_1844+60delinsATACTT	NP_683696.2:n.1844+55_1844+60delinsATACTT
NM_148900.3:c.1820+55_1820+60delinsATACTT	NP_683698.2:n.1820+55_1820+60delinsATACTT
NR_033766.1:n.2154+55_2154+60delinsATACTT
NR_033767.1:n.2201+55_2201+60delinsATACTT
XM_011516706.1:c.1913+55_1913+60delinsATACTT	XP_011515008.1:n.1913+55_1913+60delinsATACTT
XM_017012801.2:c.1844+55_1844+60delinsATACTT	XP_016868290.1:n.1844+55_1844+60delinsATACTT
NM_014491.4:c.1769+55_1769+60delinsATACTT MANE Select	NP_055306.1:n.1769+55_1769+60delinsATACTT
NM_001172766.3:c.1766+55_1766+60delinsATACTT	NP_001166237.1:n.1766+55_1766+60delinsATACTT
NM_148898.4:c.1844+55_1844+60delinsATACTT	NP_683696.2:n.1844+55_1844+60delinsATACTT
NR_033766.2:n.2137+55_2137+60delinsATACTT
NR_033767.2:n.2383+55_2383+60delinsATACTT
NM_148900.4:c.1820+55_1820+60delinsATACTT	NP_683698.2:n.1820+55_1820+60delinsATACTT