Canonical Allele Identifier: CA1106076603

Gene: FOXP2

Linked Data

• dbSNP Id: rs1790936499
• gnomAD v3: 7-114101049-A-AG
• gnomAD v4: 7-114101049-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114101049_114101050insG , CM000669.2:g.114101049_114101050insG	GRCh38
NC_000007.13:g.113741104_113741105insG , CM000669.1:g.113741104_113741105insG	GRCh37
NC_000007.12:g.113528340_113528341insG	NCBI36
NG_007491.2:g.19740_19741insG
NG_007491.3:g.19740_19741insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703612.1:c.-247+14438_-247+14439insG	ENSP00000515396.1:n.-247+14438_-247+14439insG
ENST00000703613.1:c.-365+14438_-365+14439insG	ENSP00000515397.1:n.-365+14438_-365+14439insG
ENST00000703614.1:c.-247+14438_-247+14439insG	ENSP00000515398.1:n.-247+14438_-247+14439insG
ENST00000703615.1:c.-365+14438_-365+14439insG	ENSP00000515399.1:n.-365+14438_-365+14439insG
ENST00000703616.1:c.-247+13211_-247+13212insG	ENSP00000515400.1:n.-247+13211_-247+13212insG
ENST00000412402.5:c.-102+14438_-102+14439insG	ENSP00000405470.1:n.-102+14438_-102+14439insG
ENST00000440349.5:c.-247+14438_-247+14439insG	ENSP00000395552.1:n.-247+14438_-247+14439insG
ENST00000441290.6:c.-435+14438_-435+14439insG	ENSP00000416825.1:n.-435+14438_-435+14439insG
ENST00000495516.1:n.105+12779_105+12780insG
ENST00000635638.1:c.-247+13211_-247+13212insG	ENSP00000489073.1:n.-247+13211_-247+13212insG
NR_033766.1:n.302+14438_302+14439insG
XM_011516706.1:c.-360+14438_-360+14439insG	XP_011515008.1:n.-360+14438_-360+14439insG
XM_017012801.2:c.-247+12621_-247+12622insG	XP_016868290.1:n.-247+12621_-247+12622insG
NR_033766.2:n.285+14438_285+14439insG