Canonical Allele Identifier: CA329133742
Gene: FOXP3 HGNC NCBI

Linked Data

dbSNP Id: rs886821043
MyVariant Identifiers: chrX:g.49108170G>C (hg19) chrX:g.49251709G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49251709G>C , CM000685.2:g.49251709G>C GRCh38
NC_000023.10:g.49108170G>C , CM000685.1:g.49108170G>C GRCh37
NC_000023.9:g.48995114G>C NCBI36
NG_007392.1:g.18119C>G , LRG_62:g.18119C>G
NG_021311.2:g.21245G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376199.7:c.996C>G ENSP00000365372.2:p.Phe332Leu
ENST00000376207.10:c.1101C>G MANE Select ENSP00000365380.4:p.Phe367Leu
ENST00000455775.7:c.1170C>G ENSP00000396415.3:p.Phe390Leu
ENST00000518685.6:c.1020C>G ENSP00000428952.2:p.Phe340Leu
ENST00000557224.6:c.996C>G ENSP00000451208.1:p.Phe332Leu
ENST00000651307.1:c.*16C>G ENSP00000498454.1:n.*16C>G
ENST00000376197.1:c.951C>G ENSP00000365369.1:p.Phe317Leu
ENST00000376199.6:c.996C>G ENSP00000365372.2:p.Phe332Leu
ENST00000376207.8:c.1101C>G ENSP00000365380.4:p.Phe367Leu
ENST00000455775.6:c.1170C>G ENSP00000396415.3:p.Phe390Leu
ENST00000518685.5:c.996C>G ENSP00000428952.1:p.Phe332Leu
ENST00000557224.5:c.996C>G ENSP00000451208.1:p.Phe332Leu
NM_001114377.1:c.996C>G NP_001107849.1:p.Phe332Leu
NM_014009.3:c.1101C>G , LRG_62t1:c.1101C>G NP_054728.2:p.Phe367Leu
XM_006724533.2:c.1170C>G XP_006724596.2:p.Phe390Leu
XM_011543915.1:c.1320C>G XP_011542217.1:p.Phe440Leu
XM_011543916.1:c.1320C>G XP_011542218.1:p.Phe440Leu
XM_011543917.1:c.1119C>G XP_011542219.1:p.Phe373Leu
XM_011543918.1:c.1356C>G XP_011542220.1:p.Phe452Leu
XM_011543919.1:c.1320C>G XP_011542221.1:p.Phe440Leu
XM_017029567.1:c.1047C>G XP_016885056.1:p.Phe349Leu
NM_001114377.2:c.996C>G NP_001107849.1:p.Phe332Leu
NM_014009.4:c.1101C>G MANE Select NP_054728.2:p.Phe367Leu
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