Canonical Allele Identifier: CA165170395

Gene: FOXP2

Linked Data

• dbSNP Id: rs1043014727
• gnomAD v3: 7-114101099-C-A
• gnomAD v4: 7-114101099-C-A
• MyVariant Identifiers: chr7:g.113741154C>A (hg19) ; chr7:g.114101099C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114101099C>A , CM000669.2:g.114101099C>A	GRCh38
NC_000007.13:g.113741154C>A , CM000669.1:g.113741154C>A	GRCh37
NC_000007.12:g.113528390C>A	NCBI36
NG_007491.2:g.19790C>A
NG_007491.3:g.19790C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703612.1:c.-247+14488C>A	ENSP00000515396.1:n.-247+14488C>A
ENST00000703613.1:c.-365+14488C>A	ENSP00000515397.1:n.-365+14488C>A
ENST00000703614.1:c.-247+14488C>A	ENSP00000515398.1:n.-247+14488C>A
ENST00000703615.1:c.-365+14488C>A	ENSP00000515399.1:n.-365+14488C>A
ENST00000703616.1:c.-247+13261C>A	ENSP00000515400.1:n.-247+13261C>A
ENST00000412402.5:c.-102+14488C>A	ENSP00000405470.1:n.-102+14488C>A
ENST00000440349.5:c.-247+14488C>A	ENSP00000395552.1:n.-247+14488C>A
ENST00000441290.6:c.-435+14488C>A	ENSP00000416825.1:n.-435+14488C>A
ENST00000495516.1:n.105+12829C>A
ENST00000635638.1:c.-247+13261C>A	ENSP00000489073.1:n.-247+13261C>A
NR_033766.1:n.302+14488C>A
XM_011516706.1:c.-360+14488C>A	XP_011515008.1:n.-360+14488C>A
XM_017012801.2:c.-247+12671C>A	XP_016868290.1:n.-247+12671C>A
NR_033766.2:n.285+14488C>A