Canonical Allele Identifier: CA1736032038

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114689921_114689932del , CM000669.2:g.114689921_114689932del	GRCh38
NC_000007.13:g.114329976_114329987del , CM000669.1:g.114329976_114329987del	GRCh37
NC_000007.12:g.114117212_114117223del	NCBI36
NG_007491.2:g.608612_608623del
NG_007491.3:g.608612_608623del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.2194_*6del	ENSP00000385069.4:n.[c.2194_*6del;Glu732ThrfsTer7]
ENST00000703612.1:c.2134_*6del	ENSP00000515396.1:n.[c.2134_*6del;Glu712ThrfsTer7]
ENST00000703613.1:c.2194_*6del	ENSP00000515397.1:n.[c.2194_*6del;Glu732ThrfsTer7]
ENST00000703614.1:c.2143_*6del	ENSP00000515398.1:n.[c.2143_*6del;Glu715ThrfsTer7]
ENST00000703616.1:c.2269_*6del	ENSP00000515400.1:n.[c.2269_*6del;Glu757ThrfsTer7]
ENST00000350908.9:c.2143_*6del MANE Select	ENSP00000265436.7:n.[c.2143_*6del;Glu715ThrfsTer7]
ENST00000393489.8:c.*1937_*1948del	ENSP00000377129.4:n.*1937_*1948del
ENST00000350908.8:c.2143_*6del	ENSP00000265436.7:n.[c.2143_*6del;Glu715ThrfsTer7]
ENST00000393489.7:c.1867_*6del	ENSP00000377129.3:n.[c.1867_*6del;Glu623ThrfsTer7]
ENST00000393491.7:c.1588_*6del	ENSP00000377130.3:n.[c.1588_*6del;Glu530ThrfsTer7]
ENST00000393494.6:c.2143_*6del	ENSP00000377132.2:n.[c.2143_*6del;Glu715ThrfsTer7]
ENST00000393498.6:c.2080_*6del	ENSP00000377135.2:n.[c.2080_*6del;Glu694ThrfsTer7]
ENST00000403559.8:c.2194_*6del	ENSP00000385069.4:n.[c.2194_*6del;Glu732ThrfsTer7]
ENST00000408937.7:c.2218_*6del	ENSP00000386200.3:n.[c.2218_*6del;Glu740ThrfsTer7]
ENST00000412402.5:c.*1861_*1872del	ENSP00000405470.1:n.*1861_*1872del
ENST00000634411.1:c.2092_*6del	ENSP00000489135.1:n.[c.2092_*6del;Glu698ThrfsTer7]
ENST00000634664.1:n.618_629del
ENST00000635109.1:c.*1940_*1951del	ENSP00000489457.1:n.*1940_*1951del
ENST00000635534.1:c.2134_*6del	ENSP00000489229.1:n.[c.2134_*6del;Glu712ThrfsTer7]
ENST00000635638.1:c.2146_*6del	ENSP00000489073.1:n.[c.2146_*6del;Glu716ThrfsTer7]
NM_001172766.2:c.2140_*6del	NP_001166237.1:n.[c.2140_*6del;Glu714ThrfsTer7]
NM_014491.3:c.2143_*6del	NP_055306.1:n.[c.2143_*6del;Glu715ThrfsTer7]
NM_148898.3:c.2218_*6del	NP_683696.2:n.[c.2218_*6del;Glu740ThrfsTer7]
NM_148900.3:c.2194_*6del	NP_683698.2:n.[c.2194_*6del;Glu732ThrfsTer7]
NR_033766.1:n.2528_2539del
NR_033767.1:n.2575_2586del
XM_011516706.1:c.2287_*6del	XP_011515008.1:n.[c.2287_*6del;Glu763ThrfsTer7]
XM_017012801.2:c.2218_*6del	XP_016868290.1:n.[c.2218_*6del;Glu740ThrfsTer7]
NM_014491.4:c.2143_*6del MANE Select	NP_055306.1:n.[c.2143_*6del;Glu715ThrfsTer7]
NM_001172766.3:c.2140_*6del	NP_001166237.1:n.[c.2140_*6del;Glu714ThrfsTer7]
NM_148898.4:c.2218_*6del	NP_683696.2:n.[c.2218_*6del;Glu740ThrfsTer7]
NR_033766.2:n.2511_2522del
NR_033767.2:n.2757_2768del
NM_148900.4:c.2194_*6del	NP_683698.2:n.[c.2194_*6del;Glu732ThrfsTer7]