Canonical Allele Identifier: CA1106106770

Gene: FOXP2

Linked Data

• dbSNP Id: rs1212735188
• gnomAD v3: 7-114662005-G-A
• gnomAD v4: 7-114662005-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662005G>A , CM000669.2:g.114662005G>A	GRCh38
NC_000007.13:g.114302060G>A , CM000669.1:g.114302060G>A	GRCh37
NC_000007.12:g.114089296G>A	NCBI36
NG_007491.2:g.580696G>A
NG_007491.3:g.580696G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1699-60G>A	ENSP00000385069.4:n.1699-60G>A
ENST00000703612.1:c.1639-60G>A	ENSP00000515396.1:n.1639-60G>A
ENST00000703613.1:c.1699-60G>A	ENSP00000515397.1:n.1699-60G>A
ENST00000703614.1:c.1648-60G>A	ENSP00000515398.1:n.1648-60G>A
ENST00000703616.1:c.1774-60G>A	ENSP00000515400.1:n.1774-60G>A
ENST00000703617.1:c.1093-60G>A	ENSP00000515401.1:n.1093-60G>A
ENST00000703618.1:c.545-60G>A
ENST00000350908.9:c.1648-60G>A MANE Select	ENSP00000265436.7:n.1648-60G>A
ENST00000393489.8:c.*1442-60G>A	ENSP00000377129.4:n.*1442-60G>A
ENST00000350908.8:c.1648-60G>A	ENSP00000265436.7:n.1648-60G>A
ENST00000393489.7:c.1372-60G>A	ENSP00000377129.3:n.1372-60G>A
ENST00000393491.7:c.1093-60G>A	ENSP00000377130.3:n.1093-60G>A
ENST00000393494.6:c.1648-60G>A	ENSP00000377132.2:n.1648-60G>A
ENST00000393498.6:c.1585-60G>A	ENSP00000377135.2:n.1585-60G>A
ENST00000403559.8:c.1699-60G>A	ENSP00000385069.4:n.1699-60G>A
ENST00000408937.7:c.1723-60G>A	ENSP00000386200.3:n.1723-60G>A
ENST00000412402.5:c.*1366-60G>A	ENSP00000405470.1:n.*1366-60G>A
ENST00000441290.6:c.*1648-60G>A	ENSP00000416825.1:n.*1648-60G>A
ENST00000634411.1:c.1597-60G>A	ENSP00000489135.1:n.1597-60G>A
ENST00000634623.1:c.1588-60G>A	ENSP00000488944.1:n.1588-60G>A
ENST00000634664.1:n.123-60G>A
ENST00000635109.1:c.*1445-60G>A	ENSP00000489457.1:n.*1445-60G>A
ENST00000635534.1:c.1639-60G>A	ENSP00000489229.1:n.1639-60G>A
ENST00000635638.1:c.1651-60G>A	ENSP00000489073.1:n.1651-60G>A
NM_001172766.2:c.1645-60G>A	NP_001166237.1:n.1645-60G>A
NM_014491.3:c.1648-60G>A	NP_055306.1:n.1648-60G>A
NM_148898.3:c.1723-60G>A	NP_683696.2:n.1723-60G>A
NM_148900.3:c.1699-60G>A	NP_683698.2:n.1699-60G>A
NR_033766.1:n.2033-60G>A
NR_033767.1:n.2080-60G>A
XM_011516706.1:c.1792-60G>A	XP_011515008.1:n.1792-60G>A
XM_017012801.2:c.1723-60G>A	XP_016868290.1:n.1723-60G>A
NM_014491.4:c.1648-60G>A MANE Select	NP_055306.1:n.1648-60G>A
NM_001172766.3:c.1645-60G>A	NP_001166237.1:n.1645-60G>A
NM_148898.4:c.1723-60G>A	NP_683696.2:n.1723-60G>A
NR_033766.2:n.2016-60G>A
NR_033767.2:n.2262-60G>A
NM_148900.4:c.1699-60G>A	NP_683698.2:n.1699-60G>A