Canonical Allele Identifier: CA412950291
Gene: FOXP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49253176T>A , CM000685.2:g.49253176T>A GRCh38
NC_000023.10:g.49109637T>A , CM000685.1:g.49109637T>A GRCh37
NC_000023.9:g.48996581T>A NCBI36
NG_007392.1:g.16652A>T , LRG_62:g.16652A>T
NG_021311.2:g.22712T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376199.7:c.889A>T ENSP00000365372.2:p.Lys297Ter
ENST00000376207.10:c.994A>T MANE Select ENSP00000365380.4:p.Lys332Ter
ENST00000455775.7:c.1063A>T ENSP00000396415.3:p.Lys355Ter
ENST00000518685.6:c.913A>T ENSP00000428952.2:p.Lys305Ter
ENST00000557224.6:c.889A>T ENSP00000451208.1:p.Lys297Ter
ENST00000651307.1:c.967+741A>T ENSP00000498454.1:n.967+741A>T
ENST00000376197.1:c.844A>T ENSP00000365369.1:p.Lys282Ter
ENST00000376199.6:c.889A>T ENSP00000365372.2:p.Lys297Ter
ENST00000376207.8:c.994A>T ENSP00000365380.4:p.Lys332Ter
ENST00000455775.6:c.1063A>T ENSP00000396415.3:p.Lys355Ter
ENST00000518685.5:c.889A>T ENSP00000428952.1:p.Lys297Ter
ENST00000557224.5:c.889A>T ENSP00000451208.1:p.Lys297Ter
NM_001114377.1:c.889A>T NP_001107849.1:p.Lys297Ter
NM_014009.3:c.994A>T , LRG_62t1:c.994A>T NP_054728.2:p.Lys332Ter
XM_006724533.2:c.1063A>T XP_006724596.2:p.Lys355Ter
XM_011543915.1:c.1213A>T XP_011542217.1:p.Lys405Ter
XM_011543916.1:c.1213A>T XP_011542218.1:p.Lys405Ter
XM_011543917.1:c.1012A>T XP_011542219.1:p.Lys338Ter
XM_011543918.1:c.1249A>T XP_011542220.1:p.Lys417Ter
XM_011543919.1:c.1213A>T XP_011542221.1:p.Lys405Ter
XM_017029567.1:c.940A>T XP_016885056.1:p.Lys314Ter
NM_001114377.2:c.889A>T NP_001107849.1:p.Lys297Ter
NM_014009.4:c.994A>T MANE Select NP_054728.2:p.Lys332Ter