Canonical Allele Identifier: CA1106085994

Gene: FOXP2

Linked Data

• dbSNP Id: rs1797898428
• gnomAD v3: 7-114337899-G-A
• gnomAD v4: 7-114337899-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114337899G>A , CM000669.2:g.114337899G>A	GRCh38
NC_000007.13:g.113977954G>A , CM000669.1:g.113977954G>A	GRCh37
NC_000007.12:g.113765190G>A	NCBI36
NG_007491.2:g.256590G>A
NG_007491.3:g.256590G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703612.1:c.-11+49790G>A	ENSP00000515396.1:n.-11+49790G>A
ENST00000703613.1:c.-11+49790G>A	ENSP00000515397.1:n.-11+49790G>A
ENST00000703614.1:c.-11+49790G>A	ENSP00000515398.1:n.-11+49790G>A
ENST00000703615.1:c.-11+49790G>A	ENSP00000515399.1:n.-11+49790G>A
ENST00000703616.1:c.-11+49790G>A	ENSP00000515400.1:n.-11+49790G>A
ENST00000412402.5:c.-11+49790G>A	ENSP00000405470.1:n.-11+49790G>A
ENST00000440349.5:c.-11+49790G>A	ENSP00000395552.1:n.-11+49790G>A
ENST00000441290.6:c.-146-28606G>A	ENSP00000416825.1:n.-146-28606G>A
ENST00000495516.1:n.341+49790G>A
ENST00000634411.1:c.-11+49790G>A	ENSP00000489135.1:n.-11+49790G>A
ENST00000634623.1:c.-11+49790G>A	ENSP00000488944.1:n.-11+49790G>A
ENST00000635109.1:c.-11+49790G>A	ENSP00000489457.1:n.-11+49790G>A
ENST00000635638.1:c.-11+49790G>A	ENSP00000489073.1:n.-11+49790G>A
NR_033766.1:n.393+49790G>A
XM_011516706.1:c.-11+17829G>A	XP_011515008.1:n.-11+17829G>A
XM_017012801.2:c.-11+49790G>A	XP_016868290.1:n.-11+49790G>A
NR_033766.2:n.376+49790G>A