Canonical Allele Identifier: CA2693704862
Gene: FOXP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49255429del , CM000685.2:g.49255429del GRCh38
NC_000023.10:g.49111890del , CM000685.1:g.49111890del GRCh37
NC_000023.9:g.48998834del NCBI36
NG_007392.1:g.14400del , LRG_62:g.14400del
NG_021311.2:g.24965del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376199.7:c.711+1del
ENST00000376207.10:c.816+1del
ENST00000455775.7:c.885+1del
ENST00000518685.6:c.735+287del ENSP00000428952.2:n.735+287del
ENST00000557224.6:c.711+1del
ENST00000651307.1:c.816+1del
ENST00000376197.1:c.666+1del
ENST00000376199.6:c.711+1del
ENST00000376207.8:c.816+1del
ENST00000455775.6:c.885+1del
ENST00000518685.5:c.711+1del
ENST00000557224.5:c.711+1del
NM_001114377.1:c.711+1del
NM_014009.3:c.816+1del , LRG_62t1:c.816+1del
XM_006724533.2:c.885+1del
XM_011543915.1:c.1035+1del
XM_011543916.1:c.1035+1del
XM_011543917.1:c.834+1del
XM_011543918.1:c.1071+1del
XM_011543919.1:c.1035+1del
XM_017029567.1:c.762+1del
NM_001114377.2:c.711+1del
NM_014009.4:c.816+1del