Canonical Allele Identifier: CA577215569

Gene: FOXP2

Linked Data

• dbSNP Id: rs1286088343
• gnomAD v2: 7-114299611-T-A
• gnomAD v4: 7-114659556-T-A
• MyVariant Identifiers: chr7:g.114299611T>A (hg19) ; chr7:g.114659556T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659556T>A , CM000669.2:g.114659556T>A	GRCh38
NC_000007.13:g.114299611T>A , CM000669.1:g.114299611T>A	GRCh37
NC_000007.12:g.114086847T>A	NCBI36
NG_007491.2:g.578247T>A
NG_007491.3:g.578247T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1597-16T>A	ENSP00000385069.4:n.1597-16T>A
ENST00000703612.1:c.1537-16T>A	ENSP00000515396.1:n.1537-16T>A
ENST00000703613.1:c.1597-16T>A	ENSP00000515397.1:n.1597-16T>A
ENST00000703614.1:c.1546-16T>A	ENSP00000515398.1:n.1546-16T>A
ENST00000703616.1:c.1672-16T>A	ENSP00000515400.1:n.1672-16T>A
ENST00000703617.1:c.991-16T>A	ENSP00000515401.1:n.991-16T>A
ENST00000703618.1:c.545-2509T>A
ENST00000350908.9:c.1546-16T>A MANE Select	ENSP00000265436.7:n.1546-16T>A
ENST00000393489.8:c.*1340-16T>A	ENSP00000377129.4:n.*1340-16T>A
ENST00000350908.8:c.1546-16T>A	ENSP00000265436.7:n.1546-16T>A
ENST00000393489.7:c.1270-16T>A	ENSP00000377129.3:n.1270-16T>A
ENST00000393491.7:c.991-16T>A	ENSP00000377130.3:n.991-16T>A
ENST00000393494.6:c.1546-16T>A	ENSP00000377132.2:n.1546-16T>A
ENST00000393498.6:c.1483-16T>A	ENSP00000377135.2:n.1483-16T>A
ENST00000403559.8:c.1597-16T>A	ENSP00000385069.4:n.1597-16T>A
ENST00000408937.7:c.1621-16T>A	ENSP00000386200.3:n.1621-16T>A
ENST00000412402.5:c.*1264-16T>A	ENSP00000405470.1:n.*1264-16T>A
ENST00000441290.6:c.*1546-16T>A	ENSP00000416825.1:n.*1546-16T>A
ENST00000634411.1:c.1495-16T>A	ENSP00000489135.1:n.1495-16T>A
ENST00000634623.1:c.1486-16T>A	ENSP00000488944.1:n.1486-16T>A
ENST00000635109.1:c.*1343-16T>A	ENSP00000489457.1:n.*1343-16T>A
ENST00000635534.1:c.1537-16T>A	ENSP00000489229.1:n.1537-16T>A
ENST00000635638.1:c.1549-16T>A	ENSP00000489073.1:n.1549-16T>A
NM_001172766.2:c.1543-16T>A	NP_001166237.1:n.1543-16T>A
NM_014491.3:c.1546-16T>A	NP_055306.1:n.1546-16T>A
NM_148898.3:c.1621-16T>A	NP_683696.2:n.1621-16T>A
NM_148900.3:c.1597-16T>A	NP_683698.2:n.1597-16T>A
NR_033766.1:n.1931-16T>A
NR_033767.1:n.1978-16T>A
XM_011516706.1:c.1690-16T>A	XP_011515008.1:n.1690-16T>A
XM_017012801.2:c.1621-16T>A	XP_016868290.1:n.1621-16T>A
NM_014491.4:c.1546-16T>A MANE Select	NP_055306.1:n.1546-16T>A
NM_001172766.3:c.1543-16T>A	NP_001166237.1:n.1543-16T>A
NM_148898.4:c.1621-16T>A	NP_683696.2:n.1621-16T>A
NR_033766.2:n.1914-16T>A
NR_033767.2:n.2160-16T>A
NM_148900.4:c.1597-16T>A	NP_683698.2:n.1597-16T>A