Canonical Allele Identifier: CA412951088

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49112193G>A (hg19) ; chrX:g.49255732G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255732G>A , CM000685.2:g.49255732G>A	GRCh38
NC_000023.10:g.49112193G>A , CM000685.1:g.49112193G>A	GRCh37
NC_000023.9:g.48999137G>A	NCBI36
NG_007392.1:g.14096C>T , LRG_62:g.14096C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.613C>T	ENSP00000365372.2:p.Gln205Ter
ENST00000376207.10:c.718C>T MANE Select	ENSP00000365380.4:p.Gln240Ter
ENST00000455775.7:c.787C>T	ENSP00000396415.3:p.Gln263Ter
ENST00000518685.6:c.718C>T	ENSP00000428952.2:p.Gln240Ter
ENST00000557224.6:c.613C>T	ENSP00000451208.1:p.Gln205Ter
ENST00000651307.1:c.718C>T	ENSP00000498454.1:p.Gln240Ter
ENST00000376197.1:c.568C>T	ENSP00000365369.1:p.Gln190Ter
ENST00000376199.6:c.613C>T	ENSP00000365372.2:p.Gln205Ter
ENST00000376207.8:c.718C>T	ENSP00000365380.4:p.Gln240Ter
ENST00000455775.6:c.787C>T	ENSP00000396415.3:p.Gln263Ter
ENST00000518685.5:c.613C>T	ENSP00000428952.1:p.Gln205Ter
ENST00000557224.5:c.613C>T	ENSP00000451208.1:p.Gln205Ter
NM_001114377.1:c.613C>T	NP_001107849.1:p.Gln205Ter
NM_014009.3:c.718C>T , LRG_62t1:c.718C>T	NP_054728.2:p.Gln240Ter
XM_006724533.2:c.787C>T	XP_006724596.2:p.Gln263Ter
XM_011543915.1:c.937C>T	XP_011542217.1:p.Gln313Ter
XM_011543916.1:c.937C>T	XP_011542218.1:p.Gln313Ter
XM_011543917.1:c.736C>T	XP_011542219.1:p.Gln246Ter
XM_011543918.1:c.973C>T	XP_011542220.1:p.Gln325Ter
XM_011543919.1:c.937C>T	XP_011542221.1:p.Gln313Ter
XM_017029567.1:c.664C>T	XP_016885056.1:p.Gln222Ter
NM_001114377.2:c.613C>T	NP_001107849.1:p.Gln205Ter
NM_014009.4:c.718C>T MANE Select	NP_054728.2:p.Gln240Ter