Canonical Allele Identifier: CA412951017
Gene: FOXP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49255500C>T , CM000685.2:g.49255500C>T GRCh38
NC_000023.10:g.49111961C>T , CM000685.1:g.49111961C>T GRCh37
NC_000023.9:g.48998905C>T NCBI36
NG_007392.1:g.14328G>A , LRG_62:g.14328G>A
NG_021311.2:g.25036C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376199.7:c.640G>A ENSP00000365372.2:p.Glu214Lys
ENST00000376207.10:c.745G>A MANE Select ENSP00000365380.4:p.Glu249Lys
ENST00000455775.7:c.814G>A ENSP00000396415.3:p.Glu272Lys
ENST00000518685.6:c.735+215G>A ENSP00000428952.2:n.735+215G>A
ENST00000557224.6:c.640G>A ENSP00000451208.1:p.Glu214Lys
ENST00000651307.1:c.745G>A ENSP00000498454.1:p.Glu249Lys
ENST00000376197.1:c.595G>A ENSP00000365369.1:p.Glu199Lys
ENST00000376199.6:c.640G>A ENSP00000365372.2:p.Glu214Lys
ENST00000376207.8:c.745G>A ENSP00000365380.4:p.Glu249Lys
ENST00000455775.6:c.814G>A ENSP00000396415.3:p.Glu272Lys
ENST00000518685.5:c.640G>A ENSP00000428952.1:p.Glu214Lys
ENST00000557224.5:c.640G>A ENSP00000451208.1:p.Glu214Lys
NM_001114377.1:c.640G>A NP_001107849.1:p.Glu214Lys
NM_014009.3:c.745G>A , LRG_62t1:c.745G>A NP_054728.2:p.Glu249Lys
XM_006724533.2:c.814G>A XP_006724596.2:p.Glu272Lys
XM_011543915.1:c.964G>A XP_011542217.1:p.Glu322Lys
XM_011543916.1:c.964G>A XP_011542218.1:p.Glu322Lys
XM_011543917.1:c.763G>A XP_011542219.1:p.Glu255Lys
XM_011543918.1:c.1000G>A XP_011542220.1:p.Glu334Lys
XM_011543919.1:c.964G>A XP_011542221.1:p.Glu322Lys
XM_017029567.1:c.691G>A XP_016885056.1:p.Glu231Lys
NM_001114377.2:c.640G>A NP_001107849.1:p.Glu214Lys
NM_014009.4:c.745G>A MANE Select NP_054728.2:p.Glu249Lys