Canonical Allele Identifier: CA2428552712
Gene: FOXP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49255722_49255723delinsTC , CM000685.2:g.49255722_49255723delinsTC GRCh38
NC_000023.10:g.49112183_49112184delinsTC , CM000685.1:g.49112183_49112184delinsTC GRCh37
NC_000023.9:g.48999127_48999128delinsTC NCBI36
NG_007392.1:g.14105_14106delinsGA , LRG_62:g.14105_14106delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000376199.7:c.622_623delinsGA ENSP00000365372.2:p.Glu208=
ENST00000376207.10:c.727_728delinsGA MANE Select ENSP00000365380.4:p.Glu243=
ENST00000455775.7:c.796_797delinsGA ENSP00000396415.3:p.Glu266=
ENST00000518685.6:c.727_728delinsGA ENSP00000428952.2:p.Glu243=
ENST00000557224.6:c.622_623delinsGA ENSP00000451208.1:p.Glu208=
ENST00000651307.1:c.727_728delinsGA ENSP00000498454.1:p.Glu243=
ENST00000376197.1:c.577_578delinsGA ENSP00000365369.1:p.Glu193=
ENST00000376199.6:c.622_623delinsGA ENSP00000365372.2:p.Glu208=
ENST00000376207.8:c.727_728delinsGA ENSP00000365380.4:p.Glu243=
ENST00000455775.6:c.796_797delinsGA ENSP00000396415.3:p.Glu266=
ENST00000518685.5:c.622_623delinsGA ENSP00000428952.1:p.Glu208=
ENST00000557224.5:c.622_623delinsGA ENSP00000451208.1:p.Glu208=
NM_001114377.1:c.622_623delinsGA NP_001107849.1:p.Glu208=
NM_014009.3:c.727_728delinsGA , LRG_62t1:c.727_728delinsGA NP_054728.2:p.Glu243=
XM_006724533.2:c.796_797delinsGA XP_006724596.2:p.Glu266=
XM_011543915.1:c.946_947delinsGA XP_011542217.1:p.Glu316=
XM_011543916.1:c.946_947delinsGA XP_011542218.1:p.Glu316=
XM_011543917.1:c.745_746delinsGA XP_011542219.1:p.Glu249=
XM_011543918.1:c.982_983delinsGA XP_011542220.1:p.Glu328=
XM_011543919.1:c.946_947delinsGA XP_011542221.1:p.Glu316=
XM_017029567.1:c.673_674delinsGA XP_016885056.1:p.Glu225=
NM_001114377.2:c.622_623delinsGA NP_001107849.1:p.Glu208=
NM_014009.4:c.727_728delinsGA MANE Select NP_054728.2:p.Glu243=