Canonical Allele Identifier: CA2428553325

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49257483G= , CM000685.2:g.49257483G=	GRCh38
NC_000023.10:g.49113940G= , CM000685.1:g.49113940G=	GRCh37
NC_000023.9:g.49000884G=	NCBI36
NG_007392.1:g.12349C= , LRG_62:g.12349C=

Transcript Alleles

HGVS	Amino-acid Change
NM_014009.4:c.398C= MANE Select	NP_054728.2:p.Pro133=
ENST00000376207.10:c.398C= MANE Select	ENSP00000365380.4:p.Pro133=
NM_001114377.1:c.293C=	NP_001107849.1:p.Pro98=
NM_001114377.2:c.293C=	NP_001107849.1:p.Pro98=
NM_014009.3:c.398C= , LRG_62t1:c.398C=	NP_054728.2:p.Pro133=
ENST00000376197.1:c.248C=	ENSP00000365369.1:p.Pro83=
ENST00000376199.6:c.293C=	ENSP00000365372.2:p.Pro98=
ENST00000376199.7:c.293C=	ENSP00000365372.2:p.Pro98=
ENST00000376207.8:c.398C=	ENSP00000365380.4:p.Pro133=
ENST00000455775.6:c.398C=	ENSP00000396415.3:p.Pro133=
ENST00000455775.7:c.398C=	ENSP00000396415.3:p.Pro133=
ENST00000518685.5:c.293C=	ENSP00000428952.1:p.Pro98=
ENST00000518685.6:c.398C=	ENSP00000428952.2:p.Pro133=
ENST00000557224.5:c.293C=	ENSP00000451208.1:p.Pro98=
ENST00000557224.6:c.293C=	ENSP00000451208.1:p.Pro98=
ENST00000651307.1:c.398C=	ENSP00000498454.1:p.Pro133=
ENST00000652559.1:c.251C=	ENSP00000498236.1:p.Pro84=
XM_006724533.2:c.398C=	XP_006724596.2:p.Pro133=
XM_011543915.1:c.617C=	XP_011542217.1:p.Pro206=
XM_011543916.1:c.617C=	XP_011542218.1:p.Pro206=
XM_011543917.1:c.416C=	XP_011542219.1:p.Pro139=
XM_011543918.1:c.653C=	XP_011542220.1:p.Pro218=
XM_011543919.1:c.617C=	XP_011542221.1:p.Pro206=
XM_017029567.1:c.344C=	XP_016885056.1:p.Pro115=