Canonical Allele Identifier: CA412947639

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49107916T>G (hg19) ; chrX:g.49251455T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251455T>G , CM000685.2:g.49251455T>G	GRCh38
NC_000023.10:g.49107916T>G , CM000685.1:g.49107916T>G	GRCh37
NC_000023.9:g.48994860T>G	NCBI36
NG_007392.1:g.18373A>C , LRG_62:g.18373A>C
NG_021311.2:g.20991T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.1070A>C	ENSP00000365372.2:p.His357Pro
ENST00000376207.10:c.1175A>C MANE Select	ENSP00000365380.4:p.His392Pro
ENST00000455775.7:c.1244A>C	ENSP00000396415.3:p.His415Pro
ENST00000518685.6:c.1094A>C	ENSP00000428952.2:p.His365Pro
ENST00000557224.6:c.1250A>C	ENSP00000451208.1:p.His417Pro
ENST00000651307.1:c.*90A>C	ENSP00000498454.1:n.*90A>C
ENST00000376197.1:c.1205A>C	ENSP00000365369.1:p.His402Pro
ENST00000376199.6:c.1070A>C	ENSP00000365372.2:p.His357Pro
ENST00000376207.8:c.1175A>C	ENSP00000365380.4:p.His392Pro
ENST00000455775.6:c.1244A>C	ENSP00000396415.3:p.His415Pro
ENST00000518685.5:c.1070A>C	ENSP00000428952.1:p.His357Pro
ENST00000557224.5:c.1250A>C	ENSP00000451208.1:p.His417Pro
NM_001114377.1:c.1070A>C	NP_001107849.1:p.His357Pro
NM_014009.3:c.1175A>C , LRG_62t1:c.1175A>C	NP_054728.2:p.His392Pro
XM_006724533.2:c.1244A>C	XP_006724596.2:p.His415Pro
XM_011543915.1:c.1574A>C	XP_011542217.1:p.His525Pro
XM_011543916.1:c.1574A>C	XP_011542218.1:p.His525Pro
XM_011543917.1:c.1193A>C	XP_011542219.1:p.His398Pro
XM_011543918.1:c.1430A>C	XP_011542220.1:p.His477Pro
XM_011543919.1:c.1394A>C	XP_011542221.1:p.His465Pro
XM_017029567.1:c.1301A>C	XP_016885056.1:p.His434Pro
NM_001114377.2:c.1070A>C	NP_001107849.1:p.His357Pro
NM_014009.4:c.1175A>C MANE Select	NP_054728.2:p.His392Pro