Canonical Allele Identifier: CA577213854

Gene: FOXP2

Linked Data

• dbSNP Id: rs1359199653
• gnomAD v2: 7-114292230-TTC-T
• gnomAD v4: 7-114652175-TTC-T
• MyVariant Identifiers: chr7:g.114292231_114292232del (hg19) ; chr7:g.114652176_114652177del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114652177_114652178del , CM000669.2:g.114652177_114652178del	GRCh38
NC_000007.13:g.114292232_114292233del , CM000669.1:g.114292232_114292233del	GRCh37
NC_000007.12:g.114079468_114079469del	NCBI36
NG_007491.2:g.570868_570869del
NG_007491.3:g.570868_570869del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1146-26_1146-25del	ENSP00000385069.4:n.1146-26_1146-25del
ENST00000703612.1:c.1086-26_1086-25del	ENSP00000515396.1:n.1086-26_1086-25del
ENST00000703613.1:c.1146-26_1146-25del	ENSP00000515397.1:n.1146-26_1146-25del
ENST00000703614.1:c.1095-26_1095-25del	ENSP00000515398.1:n.1095-26_1095-25del
ENST00000703616.1:c.1221-26_1221-25del	ENSP00000515400.1:n.1221-26_1221-25del
ENST00000703617.1:c.819-26_819-25del	ENSP00000515401.1:n.819-26_819-25del
ENST00000703618.1:c.373-26_373-25del
ENST00000350908.9:c.1095-26_1095-25del MANE Select	ENSP00000265436.7:n.1095-26_1095-25del
ENST00000393489.8:c.*889-26_*889-25del	ENSP00000377129.4:n.*889-26_*889-25del
ENST00000350908.8:c.1095-26_1095-25del	ENSP00000265436.7:n.1095-26_1095-25del
ENST00000360232.8:c.1095-26_1095-25del	ENSP00000353367.4:n.1095-26_1095-25del
ENST00000390668.3:c.1167-26_1167-25del	ENSP00000375084.3:n.1167-26_1167-25del
ENST00000393489.7:c.819-26_819-25del	ENSP00000377129.3:n.819-26_819-25del
ENST00000393491.7:c.819-26_819-25del	ENSP00000377130.3:n.819-26_819-25del
ENST00000393494.6:c.1095-26_1095-25del	ENSP00000377132.2:n.1095-26_1095-25del
ENST00000393498.6:c.1032-26_1032-25del	ENSP00000377135.2:n.1032-26_1032-25del
ENST00000403559.8:c.1146-26_1146-25del	ENSP00000385069.4:n.1146-26_1146-25del
ENST00000408937.7:c.1170-26_1170-25del	ENSP00000386200.3:n.1170-26_1170-25del
ENST00000412402.5:c.*1015-26_*1015-25del	ENSP00000405470.1:n.*1015-26_*1015-25del
ENST00000441290.6:c.*940-26_*940-25del	ENSP00000416825.1:n.*940-26_*940-25del
ENST00000634372.1:n.222-26_222-25del
ENST00000634411.1:c.1044-26_1044-25del	ENSP00000489135.1:n.1044-26_1044-25del
ENST00000634623.1:c.1035-26_1035-25del	ENSP00000488944.1:n.1035-26_1035-25del
ENST00000635109.1:c.*892-26_*892-25del	ENSP00000489457.1:n.*892-26_*892-25del
ENST00000635534.1:c.1086-26_1086-25del	ENSP00000489229.1:n.1086-26_1086-25del
ENST00000635563.1:c.635-26_635-25del
ENST00000635638.1:c.1098-26_1098-25del	ENSP00000489073.1:n.1098-26_1098-25del
NM_001172766.2:c.1092-26_1092-25del	NP_001166237.1:n.1092-26_1092-25del
NM_001172767.2:c.1170-26_1170-25del	NP_001166238.1:n.1170-26_1170-25del
NM_014491.3:c.1095-26_1095-25del	NP_055306.1:n.1095-26_1095-25del
NM_148898.3:c.1170-26_1170-25del	NP_683696.2:n.1170-26_1170-25del
NM_148899.3:c.1095-26_1095-25del	NP_683697.2:n.1095-26_1095-25del
NM_148900.3:c.1146-26_1146-25del	NP_683698.2:n.1146-26_1146-25del
NR_033766.1:n.1682-26_1682-25del
NR_033767.1:n.1527-26_1527-25del
XM_011516706.1:c.1239-26_1239-25del	XP_011515008.1:n.1239-26_1239-25del
XM_017012801.2:c.1170-26_1170-25del	XP_016868290.1:n.1170-26_1170-25del
NM_014491.4:c.1095-26_1095-25del MANE Select	NP_055306.1:n.1095-26_1095-25del
NM_001172766.3:c.1092-26_1092-25del	NP_001166237.1:n.1092-26_1092-25del
NM_148898.4:c.1170-26_1170-25del	NP_683696.2:n.1170-26_1170-25del
NR_033766.2:n.1665-26_1665-25del
NR_033767.2:n.1709-26_1709-25del
NM_148900.4:c.1146-26_1146-25del	NP_683698.2:n.1146-26_1146-25del