Canonical Allele Identifier: CA577213868

Gene: FOXP2

Linked Data

• dbSNP Id: rs1373735581
• gnomAD v2: 7-114292253-T-C
• gnomAD v4: 7-114652198-T-C
• MyVariant Identifiers: chr7:g.114292253T>C (hg19) ; chr7:g.114652198T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114652198T>C , CM000669.2:g.114652198T>C	GRCh38
NC_000007.13:g.114292253T>C , CM000669.1:g.114292253T>C	GRCh37
NC_000007.12:g.114079489T>C	NCBI36
NG_007491.2:g.570889T>C
NG_007491.3:g.570889T>C

Transcript Alleles

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