Canonical Allele Identifier: CA329137967
Gene: FOXP3 HGNC NCBI

Linked Data

dbSNP Id: rs3761547
gnomAD v2: X-49118461-T-C
gnomAD v3: X-49262004-T-C
gnomAD v4: X-49262004-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49262004T>C , CM000685.2:g.49262004T>C GRCh38
NC_000023.10:g.49118461T>C , CM000685.1:g.49118461T>C GRCh37
NC_000023.9:g.49005405T>C NCBI36
NG_007392.1:g.7828A>G , LRG_62:g.7828A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703450.1:c.-22-3477A>G ENSP00000515301.1:n.-22-3477A>G
ENST00000684155.1:c.-23+2657A>G ENSP00000507726.1:n.-23+2657A>G
ENST00000376199.7:c.-23+2657A>G ENSP00000365372.2:n.-23+2657A>G
ENST00000376207.10:c.-23+2657A>G MANE Select ENSP00000365380.4:n.-23+2657A>G
ENST00000455775.7:c.-23+2657A>G ENSP00000396415.3:n.-23+2657A>G
ENST00000557224.6:c.-23+2657A>G ENSP00000451208.1:n.-23+2657A>G
ENST00000650877.1:c.-22-3477A>G ENSP00000499100.1:n.-22-3477A>G
ENST00000652559.1:c.-23+2657A>G ENSP00000498236.1:n.-23+2657A>G
ENST00000376199.6:c.-23+2657A>G ENSP00000365372.2:n.-23+2657A>G
ENST00000376207.8:c.-23+2657A>G ENSP00000365380.4:n.-23+2657A>G
ENST00000455775.6:c.-23+2657A>G ENSP00000396415.3:n.-23+2657A>G
NM_001114377.1:c.-23+2657A>G NP_001107849.1:n.-23+2657A>G
NM_014009.3:c.-23+2657A>G , LRG_62t1:c.-23+2657A>G NP_054728.2:n.-23+2657A>G
XM_006724533.2:c.-23+2657A>G XP_006724596.2:n.-23+2657A>G
XM_011543915.1:c.302+2657A>G XP_011542217.1:n.302+2657A>G
XM_011543916.1:c.302+2657A>G XP_011542218.1:n.302+2657A>G
XM_011543917.1:c.-23+2657A>G XP_011542219.1:n.-23+2657A>G
XM_011543918.1:c.302+2657A>G XP_011542220.1:n.302+2657A>G
XM_011543919.1:c.302+2657A>G XP_011542221.1:n.302+2657A>G
XM_017029567.1:c.29+2527A>G XP_016885056.1:n.29+2527A>G
NM_001114377.2:c.-23+2657A>G NP_001107849.1:n.-23+2657A>G
NM_014009.4:c.-23+2657A>G MANE Select NP_054728.2:n.-23+2657A>G