Canonical Allele Identifier: CA2521248915

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253162_49253163insCGT , CM000685.2:g.49253162_49253163insCGT	GRCh38
NC_000023.10:g.49109623_49109624insCGT , CM000685.1:g.49109623_49109624insCGT	GRCh37
NC_000023.9:g.48996567_48996568insCGT	NCBI36
NG_007392.1:g.16665_16666insACG , LRG_62:g.16665_16666insACG
NG_021311.2:g.22698_22699insCGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.902_903insACG	ENSP00000365372.2:p.Met301delinsIleArg
ENST00000376207.10:c.1007_1008insACG MANE Select	ENSP00000365380.4:p.Met336delinsIleArg
ENST00000455775.7:c.1076_1077insACG	ENSP00000396415.3:p.Met359delinsIleArg
ENST00000518685.6:c.926_927insACG	ENSP00000428952.2:p.Met309delinsIleArg
ENST00000557224.6:c.902_903insACG	ENSP00000451208.1:p.Met301delinsIleArg
ENST00000651307.1:c.967+754_967+755insACG	ENSP00000498454.1:n.967+754_967+755insACG...
ENST00000376197.1:c.857_858insACG	ENSP00000365369.1:p.Met286delinsIleArg
ENST00000376199.6:c.902_903insACG	ENSP00000365372.2:p.Met301delinsIleArg
ENST00000376207.8:c.1007_1008insACG	ENSP00000365380.4:p.Met336delinsIleArg
ENST00000455775.6:c.1076_1077insACG	ENSP00000396415.3:p.Met359delinsIleArg
ENST00000518685.5:c.902_903insACG	ENSP00000428952.1:p.Met301delinsIleArg
ENST00000557224.5:c.902_903insACG	ENSP00000451208.1:p.Met301delinsIleArg
NM_001114377.1:c.902_903insACG	NP_001107849.1:p.Met301delinsIleArg
NM_014009.3:c.1007_1008insACG , LRG_62t1:c.1007_1008insACG	NP_054728.2:p.Met336delinsIleArg
XM_006724533.2:c.1076_1077insACG	XP_006724596.2:p.Met359delinsIleArg
XM_011543915.1:c.1226_1227insACG	XP_011542217.1:p.Met409delinsIleArg
XM_011543916.1:c.1226_1227insACG	XP_011542218.1:p.Met409delinsIleArg
XM_011543917.1:c.1025_1026insACG	XP_011542219.1:p.Met342delinsIleArg
XM_011543918.1:c.1262_1263insACG	XP_011542220.1:p.Met421delinsIleArg
XM_011543919.1:c.1226_1227insACG	XP_011542221.1:p.Met409delinsIleArg
XM_017029567.1:c.953_954insACG	XP_016885056.1:p.Met318delinsIleArg
NM_001114377.2:c.902_903insACG	NP_001107849.1:p.Met301delinsIleArg
NM_014009.4:c.1007_1008insACG MANE Select	NP_054728.2:p.Met336delinsIleArg