Canonical Allele Identifier: CA915523311

Gene: FOXP2

Linked Data

• dbSNP Id: rs1562964278
• gnomAD v2: 7-113741064-AAC-A
• gnomAD v3: 7-114101009-AAC-A
• gnomAD v4: 7-114101009-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114101013_114101014del , CM000669.2:g.114101013_114101014del	GRCh38
NC_000007.13:g.113741068_113741069del , CM000669.1:g.113741068_113741069del	GRCh37
NC_000007.12:g.113528304_113528305del	NCBI36
NG_007491.2:g.19704_19705del
NG_007491.3:g.19704_19705del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703612.1:c.-247+14402_-247+14403del	ENSP00000515396.1:n.-247+14402_-247+14403del
ENST00000703613.1:c.-365+14402_-365+14403del	ENSP00000515397.1:n.-365+14402_-365+14403del
ENST00000703614.1:c.-247+14402_-247+14403del	ENSP00000515398.1:n.-247+14402_-247+14403del
ENST00000703615.1:c.-365+14402_-365+14403del	ENSP00000515399.1:n.-365+14402_-365+14403del
ENST00000703616.1:c.-247+13175_-247+13176del	ENSP00000515400.1:n.-247+13175_-247+13176del
ENST00000412402.5:c.-102+14402_-102+14403del	ENSP00000405470.1:n.-102+14402_-102+14403del
ENST00000440349.5:c.-247+14402_-247+14403del	ENSP00000395552.1:n.-247+14402_-247+14403del
ENST00000441290.6:c.-435+14402_-435+14403del	ENSP00000416825.1:n.-435+14402_-435+14403del
ENST00000495516.1:n.105+12743_105+12744del
ENST00000635638.1:c.-247+13175_-247+13176del	ENSP00000489073.1:n.-247+13175_-247+13176del
NR_033766.1:n.302+14402_302+14403del
XM_011516706.1:c.-360+14402_-360+14403del	XP_011515008.1:n.-360+14402_-360+14403del
XM_017012801.2:c.-247+12585_-247+12586del	XP_016868290.1:n.-247+12585_-247+12586del
NR_033766.2:n.285+14402_285+14403del