Canonical Allele Identifier: CA2428554745

Gene: FOXP3

Linked Data

• dbSNP Id: rs2066113195

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49261974_49261976del , CM000685.2:g.49261974_49261976del	GRCh38
NC_000023.10:g.49118431_49118433del , CM000685.1:g.49118431_49118433del	GRCh37
NC_000023.9:g.49005375_49005377del	NCBI36
NG_007392.1:g.7857_7859del , LRG_62:g.7857_7859del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703450.1:c.-22-3448_-22-3446del	ENSP00000515301.1:n.-22-3448_-22-3446del
ENST00000684155.1:c.-23+2686_-23+2688del	ENSP00000507726.1:n.-23+2686_-23+2688del
ENST00000376199.7:c.-23+2686_-23+2688del	ENSP00000365372.2:n.-23+2686_-23+2688del
ENST00000376207.10:c.-23+2686_-23+2688del MANE Select	ENSP00000365380.4:n.-23+2686_-23+2688del
ENST00000455775.7:c.-23+2686_-23+2688del	ENSP00000396415.3:n.-23+2686_-23+2688del
ENST00000557224.6:c.-23+2686_-23+2688del	ENSP00000451208.1:n.-23+2686_-23+2688del
ENST00000650877.1:c.-22-3448_-22-3446del	ENSP00000499100.1:n.-22-3448_-22-3446del
ENST00000652559.1:c.-23+2686_-23+2688del	ENSP00000498236.1:n.-23+2686_-23+2688del
ENST00000376199.6:c.-23+2686_-23+2688del	ENSP00000365372.2:n.-23+2686_-23+2688del
ENST00000376207.8:c.-23+2686_-23+2688del	ENSP00000365380.4:n.-23+2686_-23+2688del
ENST00000455775.6:c.-23+2686_-23+2688del	ENSP00000396415.3:n.-23+2686_-23+2688del
NM_001114377.1:c.-23+2686_-23+2688del	NP_001107849.1:n.-23+2686_-23+2688del
NM_014009.3:c.-23+2686_-23+2688del , LRG_62t1:c.-23+2686_-23+2688del	NP_054728.2:n.-23+2686_-23+2688del
XM_006724533.2:c.-23+2686_-23+2688del	XP_006724596.2:n.-23+2686_-23+2688del
XM_011543915.1:c.302+2686_302+2688del	XP_011542217.1:n.302+2686_302+2688del
XM_011543916.1:c.302+2686_302+2688del	XP_011542218.1:n.302+2686_302+2688del
XM_011543917.1:c.-23+2686_-23+2688del	XP_011542219.1:n.-23+2686_-23+2688del
XM_011543918.1:c.302+2686_302+2688del	XP_011542220.1:n.302+2686_302+2688del
XM_011543919.1:c.302+2686_302+2688del	XP_011542221.1:n.302+2686_302+2688del
XM_017029567.1:c.29+2556_29+2558del	XP_016885056.1:n.29+2556_29+2558del
NM_001114377.2:c.-23+2686_-23+2688del	NP_001107849.1:n.-23+2686_-23+2688del
NM_014009.4:c.-23+2686_-23+2688del MANE Select	NP_054728.2:n.-23+2686_-23+2688del