Canonical Allele Identifier: CA2428552669
Gene: FOXP3 HGNC NCBI

Linked Data

dbSNP Id: rs2066064324
gnomAD v4: X-49255571-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49255571G>A , CM000685.2:g.49255571G>A GRCh38
NC_000023.10:g.49112032G>A , CM000685.1:g.49112032G>A GRCh37
NC_000023.9:g.48998976G>A NCBI36
NG_007392.1:g.14257C>T , LRG_62:g.14257C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376199.7:c.631-62C>T ENSP00000365372.2:n.631-62C>T
ENST00000376207.10:c.736-62C>T MANE Select ENSP00000365380.4:n.736-62C>T
ENST00000455775.7:c.805-62C>T ENSP00000396415.3:n.805-62C>T
ENST00000518685.6:c.735+144C>T ENSP00000428952.2:n.735+144C>T
ENST00000557224.6:c.631-62C>T ENSP00000451208.1:n.631-62C>T
ENST00000651307.1:c.736-62C>T ENSP00000498454.1:n.736-62C>T
ENST00000376197.1:c.586-62C>T ENSP00000365369.1:n.586-62C>T
ENST00000376199.6:c.631-62C>T ENSP00000365372.2:n.631-62C>T
ENST00000376207.8:c.736-62C>T ENSP00000365380.4:n.736-62C>T
ENST00000455775.6:c.805-62C>T ENSP00000396415.3:n.805-62C>T
ENST00000518685.5:c.631-62C>T ENSP00000428952.1:n.631-62C>T
ENST00000557224.5:c.631-62C>T ENSP00000451208.1:n.631-62C>T
NM_001114377.1:c.631-62C>T NP_001107849.1:n.631-62C>T
NM_014009.3:c.736-62C>T , LRG_62t1:c.736-62C>T NP_054728.2:n.736-62C>T
XM_006724533.2:c.805-62C>T XP_006724596.2:n.805-62C>T
XM_011543915.1:c.955-62C>T XP_011542217.1:n.955-62C>T
XM_011543916.1:c.955-62C>T XP_011542218.1:n.955-62C>T
XM_011543917.1:c.754-62C>T XP_011542219.1:n.754-62C>T
XM_011543918.1:c.991-62C>T XP_011542220.1:n.991-62C>T
XM_011543919.1:c.955-62C>T XP_011542221.1:n.955-62C>T
XM_017029567.1:c.682-62C>T XP_016885056.1:n.682-62C>T
NM_001114377.2:c.631-62C>T NP_001107849.1:n.631-62C>T
NM_014009.4:c.736-62C>T MANE Select NP_054728.2:n.736-62C>T