Canonical Allele Identifier: CA2684564149

Gene: FOXP2

Linked Data

• gnomAD v4: 7-114662318-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662318_114662319insA , CM000669.2:g.114662318_114662319insA	GRCh38
NC_000007.13:g.114302373_114302374insA , CM000669.1:g.114302373_114302374insA	GRCh37
NC_000007.12:g.114089609_114089610insA	NCBI36
NG_007491.2:g.581009_581010insA
NG_007491.3:g.581009_581010insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1820+132_1820+133insA	ENSP00000385069.4:n.1820+132_1820+133insA
ENST00000703612.1:c.1760+132_1760+133insA	ENSP00000515396.1:n.1760+132_1760+133insA
ENST00000703613.1:c.1820+132_1820+133insA	ENSP00000515397.1:n.1820+132_1820+133insA
ENST00000703614.1:c.1769+132_1769+133insA	ENSP00000515398.1:n.1769+132_1769+133insA
ENST00000703616.1:c.1895+132_1895+133insA	ENSP00000515400.1:n.1895+132_1895+133insA
ENST00000703617.1:c.1214+132_1214+133insA	ENSP00000515401.1:n.1214+132_1214+133insA
ENST00000703618.1:c.666+132_666+133insA
ENST00000350908.9:c.1769+132_1769+133insA MANE Select	ENSP00000265436.7:n.1769+132_1769+133insA
ENST00000393489.8:c.*1563+132_*1563+133insA	ENSP00000377129.4:n.*1563+132_*1563+133insA
ENST00000350908.8:c.1769+132_1769+133insA	ENSP00000265436.7:n.1769+132_1769+133insA
ENST00000393489.7:c.1493+132_1493+133insA	ENSP00000377129.3:n.1493+132_1493+133insA
ENST00000393491.7:c.1214+132_1214+133insA	ENSP00000377130.3:n.1214+132_1214+133insA
ENST00000393494.6:c.1769+132_1769+133insA	ENSP00000377132.2:n.1769+132_1769+133insA
ENST00000393498.6:c.1706+132_1706+133insA	ENSP00000377135.2:n.1706+132_1706+133insA
ENST00000403559.8:c.1820+132_1820+133insA	ENSP00000385069.4:n.1820+132_1820+133insA
ENST00000408937.7:c.1844+132_1844+133insA	ENSP00000386200.3:n.1844+132_1844+133insA
ENST00000412402.5:c.*1487+132_*1487+133insA	ENSP00000405470.1:n.*1487+132_*1487+133insA
ENST00000441290.6:c.*1769+132_*1769+133insA	ENSP00000416825.1:n.*1769+132_*1769+133insA
ENST00000634411.1:c.1718+132_1718+133insA	ENSP00000489135.1:n.1718+132_1718+133insA
ENST00000634623.1:c.1709+132_1709+133insA	ENSP00000488944.1:n.1709+132_1709+133insA
ENST00000634664.1:n.244+132_244+133insA
ENST00000635109.1:c.*1566+132_*1566+133insA	ENSP00000489457.1:n.*1566+132_*1566+133insA
ENST00000635534.1:c.1760+132_1760+133insA	ENSP00000489229.1:n.1760+132_1760+133insA
ENST00000635638.1:c.1772+132_1772+133insA	ENSP00000489073.1:n.1772+132_1772+133insA
NM_001172766.2:c.1766+132_1766+133insA	NP_001166237.1:n.1766+132_1766+133insA
NM_014491.3:c.1769+132_1769+133insA	NP_055306.1:n.1769+132_1769+133insA
NM_148898.3:c.1844+132_1844+133insA	NP_683696.2:n.1844+132_1844+133insA
NM_148900.3:c.1820+132_1820+133insA	NP_683698.2:n.1820+132_1820+133insA
NR_033766.1:n.2154+132_2154+133insA
NR_033767.1:n.2201+132_2201+133insA
XM_011516706.1:c.1913+132_1913+133insA	XP_011515008.1:n.1913+132_1913+133insA
XM_017012801.2:c.1844+132_1844+133insA	XP_016868290.1:n.1844+132_1844+133insA
NM_014491.4:c.1769+132_1769+133insA MANE Select	NP_055306.1:n.1769+132_1769+133insA
NM_001172766.3:c.1766+132_1766+133insA	NP_001166237.1:n.1766+132_1766+133insA
NM_148898.4:c.1844+132_1844+133insA	NP_683696.2:n.1844+132_1844+133insA
NR_033766.2:n.2137+132_2137+133insA
NR_033767.2:n.2383+132_2383+133insA
NM_148900.4:c.1820+132_1820+133insA	NP_683698.2:n.1820+132_1820+133insA