Canonical Allele Identifier: CA412950884
Gene: FOXP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49255443T>A , CM000685.2:g.49255443T>A GRCh38
NC_000023.10:g.49111904T>A , CM000685.1:g.49111904T>A GRCh37
NC_000023.9:g.48998848T>A NCBI36
NG_007392.1:g.14385A>T , LRG_62:g.14385A>T
NG_021311.2:g.24979T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376199.7:c.697A>T ENSP00000365372.2:p.Lys233Ter
ENST00000376207.10:c.802A>T MANE Select ENSP00000365380.4:p.Lys268Ter
ENST00000455775.7:c.871A>T ENSP00000396415.3:p.Lys291Ter
ENST00000518685.6:c.735+272A>T ENSP00000428952.2:n.735+272A>T
ENST00000557224.6:c.697A>T ENSP00000451208.1:p.Lys233Ter
ENST00000651307.1:c.802A>T ENSP00000498454.1:p.Lys268Ter
ENST00000376197.1:c.652A>T ENSP00000365369.1:p.Lys218Ter
ENST00000376199.6:c.697A>T ENSP00000365372.2:p.Lys233Ter
ENST00000376207.8:c.802A>T ENSP00000365380.4:p.Lys268Ter
ENST00000455775.6:c.871A>T ENSP00000396415.3:p.Lys291Ter
ENST00000518685.5:c.697A>T ENSP00000428952.1:p.Lys233Ter
ENST00000557224.5:c.697A>T ENSP00000451208.1:p.Lys233Ter
NM_001114377.1:c.697A>T NP_001107849.1:p.Lys233Ter
NM_014009.3:c.802A>T , LRG_62t1:c.802A>T NP_054728.2:p.Lys268Ter
XM_006724533.2:c.871A>T XP_006724596.2:p.Lys291Ter
XM_011543915.1:c.1021A>T XP_011542217.1:p.Lys341Ter
XM_011543916.1:c.1021A>T XP_011542218.1:p.Lys341Ter
XM_011543917.1:c.820A>T XP_011542219.1:p.Lys274Ter
XM_011543918.1:c.1057A>T XP_011542220.1:p.Lys353Ter
XM_011543919.1:c.1021A>T XP_011542221.1:p.Lys341Ter
XM_017029567.1:c.748A>T XP_016885056.1:p.Lys250Ter
NM_001114377.2:c.697A>T NP_001107849.1:p.Lys233Ter
NM_014009.4:c.802A>T MANE Select NP_054728.2:p.Lys268Ter