Canonical Allele Identifier: CA412950342

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49109647C>A (hg19) ; chrX:g.49253186C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253186C>A , CM000685.2:g.49253186C>A	GRCh38
NC_000023.10:g.49109647C>A , CM000685.1:g.49109647C>A	GRCh37
NC_000023.9:g.48996591C>A	NCBI36
NG_007392.1:g.16642G>T , LRG_62:g.16642G>T
NG_021311.2:g.22722C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.879G>T	ENSP00000365372.2:p.Met293Ile
ENST00000376207.10:c.984G>T MANE Select	ENSP00000365380.4:p.Met328Ile
ENST00000455775.7:c.1053G>T	ENSP00000396415.3:p.Met351Ile
ENST00000518685.6:c.903G>T	ENSP00000428952.2:p.Met301Ile
ENST00000557224.6:c.879G>T	ENSP00000451208.1:p.Met293Ile
ENST00000651307.1:c.967+731G>T	ENSP00000498454.1:n.967+731G>T
ENST00000376197.1:c.834G>T	ENSP00000365369.1:p.Met278Ile
ENST00000376199.6:c.879G>T	ENSP00000365372.2:p.Met293Ile
ENST00000376207.8:c.984G>T	ENSP00000365380.4:p.Met328Ile
ENST00000455775.6:c.1053G>T	ENSP00000396415.3:p.Met351Ile
ENST00000518685.5:c.879G>T	ENSP00000428952.1:p.Met293Ile
ENST00000557224.5:c.879G>T	ENSP00000451208.1:p.Met293Ile
NM_001114377.1:c.879G>T	NP_001107849.1:p.Met293Ile
NM_014009.3:c.984G>T , LRG_62t1:c.984G>T	NP_054728.2:p.Met328Ile
XM_006724533.2:c.1053G>T	XP_006724596.2:p.Met351Ile
XM_011543915.1:c.1203G>T	XP_011542217.1:p.Met401Ile
XM_011543916.1:c.1203G>T	XP_011542218.1:p.Met401Ile
XM_011543917.1:c.1002G>T	XP_011542219.1:p.Met334Ile
XM_011543918.1:c.1239G>T	XP_011542220.1:p.Met413Ile
XM_011543919.1:c.1203G>T	XP_011542221.1:p.Met401Ile
XM_017029567.1:c.930G>T	XP_016885056.1:p.Met310Ile
NM_001114377.2:c.879G>T	NP_001107849.1:p.Met293Ile
NM_014009.4:c.984G>T MANE Select	NP_054728.2:p.Met328Ile