Canonical Allele Identifier: CA1736048016

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662468_114662472delinsTAGAG , CM000669.2:g.114662468_114662472delinsTAGAG	GRCh38
NC_000007.13:g.114302523_114302527delinsTAGAG , CM000669.1:g.114302523_114302527delinsTAGAG	GRCh37
NC_000007.12:g.114089759_114089763delinsTAGAG	NCBI36
NG_007491.2:g.581159_581163delinsTAGAG
NG_007491.3:g.581159_581163delinsTAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1820+282_1820+286delinsTAGAG	ENSP00000385069.4:n.1820+282_1820+286delinsTAGAG
ENST00000703612.1:c.1760+282_1760+286delinsTAGAG	ENSP00000515396.1:n.1760+282_1760+286delinsTAGAG
ENST00000703613.1:c.1820+282_1820+286delinsTAGAG	ENSP00000515397.1:n.1820+282_1820+286delinsTAGAG
ENST00000703614.1:c.1769+282_1769+286delinsTAGAG	ENSP00000515398.1:n.1769+282_1769+286delinsTAGAG
ENST00000703616.1:c.1895+282_1895+286delinsTAGAG	ENSP00000515400.1:n.1895+282_1895+286delinsTAGAG
ENST00000703617.1:c.1214+282_1214+286delinsTAGAG	ENSP00000515401.1:n.1214+282_1214+286delinsTAGAG
ENST00000703618.1:c.666+282_666+286delinsTAGAG
ENST00000350908.9:c.1769+282_1769+286delinsTAGAG MANE Select	ENSP00000265436.7:n.1769+282_1769+286delinsTAGAG
ENST00000393489.8:c.*1563+282_*1563+286delinsTAGAG	ENSP00000377129.4:n.*1563+282_*1563+286delinsTAGAG
ENST00000350908.8:c.1769+282_1769+286delinsTAGAG	ENSP00000265436.7:n.1769+282_1769+286delinsTAGAG
ENST00000393489.7:c.1493+282_1493+286delinsTAGAG	ENSP00000377129.3:n.1493+282_1493+286delinsTAGAG
ENST00000393491.7:c.1214+282_1214+286delinsTAGAG	ENSP00000377130.3:n.1214+282_1214+286delinsTAGAG
ENST00000393494.6:c.1769+282_1769+286delinsTAGAG	ENSP00000377132.2:n.1769+282_1769+286delinsTAGAG
ENST00000393498.6:c.1706+282_1706+286delinsTAGAG	ENSP00000377135.2:n.1706+282_1706+286delinsTAGAG
ENST00000403559.8:c.1820+282_1820+286delinsTAGAG	ENSP00000385069.4:n.1820+282_1820+286delinsTAGAG
ENST00000408937.7:c.1844+282_1844+286delinsTAGAG	ENSP00000386200.3:n.1844+282_1844+286delinsTAGAG
ENST00000412402.5:c.*1487+282_*1487+286delinsTAGAG	ENSP00000405470.1:n.*1487+282_*1487+286delinsTAGAG
ENST00000441290.6:c.*1769+282_*1769+286delinsTAGAG	ENSP00000416825.1:n.*1769+282_*1769+286delinsTAGAG
ENST00000634411.1:c.1718+282_1718+286delinsTAGAG	ENSP00000489135.1:n.1718+282_1718+286delinsTAGAG
ENST00000634623.1:c.1709+282_1709+286delinsTAGAG	ENSP00000488944.1:n.1709+282_1709+286delinsTAGAG
ENST00000634664.1:n.244+282_244+286delinsTAGAG
ENST00000635109.1:c.*1566+282_*1566+286delinsTAGAG	ENSP00000489457.1:n.*1566+282_*1566+286delinsTAGAG
ENST00000635534.1:c.1760+282_1760+286delinsTAGAG	ENSP00000489229.1:n.1760+282_1760+286delinsTAGAG
ENST00000635638.1:c.1772+282_1772+286delinsTAGAG	ENSP00000489073.1:n.1772+282_1772+286delinsTAGAG
NM_001172766.2:c.1766+282_1766+286delinsTAGAG	NP_001166237.1:n.1766+282_1766+286delinsTAGAG
NM_014491.3:c.1769+282_1769+286delinsTAGAG	NP_055306.1:n.1769+282_1769+286delinsTAGAG
NM_148898.3:c.1844+282_1844+286delinsTAGAG	NP_683696.2:n.1844+282_1844+286delinsTAGAG
NM_148900.3:c.1820+282_1820+286delinsTAGAG	NP_683698.2:n.1820+282_1820+286delinsTAGAG
NR_033766.1:n.2154+282_2154+286delinsTAGAG
NR_033767.1:n.2201+282_2201+286delinsTAGAG
XM_011516706.1:c.1913+282_1913+286delinsTAGAG	XP_011515008.1:n.1913+282_1913+286delinsTAGAG
XM_017012801.2:c.1844+282_1844+286delinsTAGAG	XP_016868290.1:n.1844+282_1844+286delinsTAGAG
NM_014491.4:c.1769+282_1769+286delinsTAGAG MANE Select	NP_055306.1:n.1769+282_1769+286delinsTAGAG
NM_001172766.3:c.1766+282_1766+286delinsTAGAG	NP_001166237.1:n.1766+282_1766+286delinsTAGAG
NM_148898.4:c.1844+282_1844+286delinsTAGAG	NP_683696.2:n.1844+282_1844+286delinsTAGAG
NR_033766.2:n.2137+282_2137+286delinsTAGAG
NR_033767.2:n.2383+282_2383+286delinsTAGAG
NM_148900.4:c.1820+282_1820+286delinsTAGAG	NP_683698.2:n.1820+282_1820+286delinsTAGAG