Canonical Allele Identifier: CA1735785342

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114101009_114101011delinsAAC , CM000669.2:g.114101009_114101011delinsAAC	GRCh38
NC_000007.13:g.113741064_113741066delinsAAC , CM000669.1:g.113741064_113741066delinsAAC	GRCh37
NC_000007.12:g.113528300_113528302delinsAAC	NCBI36
NG_007491.2:g.19700_19702delinsAAC
NG_007491.3:g.19700_19702delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703612.1:c.-247+14398_-247+14400delinsAAC	ENSP00000515396.1:n.-247+14398_-247+14400delinsAAC
ENST00000703613.1:c.-365+14398_-365+14400delinsAAC	ENSP00000515397.1:n.-365+14398_-365+14400delinsAAC
ENST00000703614.1:c.-247+14398_-247+14400delinsAAC	ENSP00000515398.1:n.-247+14398_-247+14400delinsAAC
ENST00000703615.1:c.-365+14398_-365+14400delinsAAC	ENSP00000515399.1:n.-365+14398_-365+14400delinsAAC
ENST00000703616.1:c.-247+13171_-247+13173delinsAAC	ENSP00000515400.1:n.-247+13171_-247+13173delinsAAC
ENST00000412402.5:c.-102+14398_-102+14400delinsAAC	ENSP00000405470.1:n.-102+14398_-102+14400delinsAAC
ENST00000440349.5:c.-247+14398_-247+14400delinsAAC	ENSP00000395552.1:n.-247+14398_-247+14400delinsAAC
ENST00000441290.6:c.-435+14398_-435+14400delinsAAC	ENSP00000416825.1:n.-435+14398_-435+14400delinsAAC
ENST00000495516.1:n.105+12739_105+12741delinsAAC
ENST00000635638.1:c.-247+13171_-247+13173delinsAAC	ENSP00000489073.1:n.-247+13171_-247+13173delinsAAC
NR_033766.1:n.302+14398_302+14400delinsAAC
XM_011516706.1:c.-360+14398_-360+14400delinsAAC	XP_011515008.1:n.-360+14398_-360+14400delinsAAC
XM_017012801.2:c.-247+12581_-247+12583delinsAAC	XP_016868290.1:n.-247+12581_-247+12583delinsAAC
NR_033766.2:n.285+14398_285+14400delinsAAC