Canonical Allele Identifier: CA2693705078

Gene: FOXP3

Linked Data

• gnomAD v4: X-49255626-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255627del , CM000685.2:g.49255627del	GRCh38
NC_000023.10:g.49112088del , CM000685.1:g.49112088del	GRCh37
NC_000023.9:g.48999032del	NCBI36
NG_007392.1:g.14201del , LRG_62:g.14201del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.630+88del	ENSP00000365372.2:n.630+88del
ENST00000376207.10:c.735+88del MANE Select	ENSP00000365380.4:n.735+88del
ENST00000455775.7:c.804+88del	ENSP00000396415.3:n.804+88del
ENST00000518685.6:c.735+88del	ENSP00000428952.2:n.735+88del
ENST00000557224.6:c.630+88del	ENSP00000451208.1:n.630+88del
ENST00000651307.1:c.735+88del	ENSP00000498454.1:n.735+88del
ENST00000376197.1:c.585+88del	ENSP00000365369.1:n.585+88del
ENST00000376199.6:c.630+88del	ENSP00000365372.2:n.630+88del
ENST00000376207.8:c.735+88del	ENSP00000365380.4:n.735+88del
ENST00000455775.6:c.804+88del	ENSP00000396415.3:n.804+88del
ENST00000518685.5:c.630+88del	ENSP00000428952.1:n.630+88del
ENST00000557224.5:c.630+88del	ENSP00000451208.1:n.630+88del
NM_001114377.1:c.630+88del	NP_001107849.1:n.630+88del
NM_014009.3:c.735+88del , LRG_62t1:c.735+88del	NP_054728.2:n.735+88del
XM_006724533.2:c.804+88del	XP_006724596.2:n.804+88del
XM_011543915.1:c.954+88del	XP_011542217.1:n.954+88del
XM_011543916.1:c.954+88del	XP_011542218.1:n.954+88del
XM_011543917.1:c.753+88del	XP_011542219.1:n.753+88del
XM_011543918.1:c.990+88del	XP_011542220.1:n.990+88del
XM_011543919.1:c.954+88del	XP_011542221.1:n.954+88del
XM_017029567.1:c.681+88del	XP_016885056.1:n.681+88del
NM_001114377.2:c.630+88del	NP_001107849.1:n.630+88del
NM_014009.4:c.735+88del MANE Select	NP_054728.2:n.735+88del