Canonical Allele Identifier: CA3164016

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs140068026
• ExAC: 4:187207595 T / A
• gnomAD v2: 4-187207595-T-A
• gnomAD v3: 4-186286441-T-A
• gnomAD v4: 4-186286441-T-A
• MyVariant Identifiers: chr4:g.187207595T>A (hg19) ; chr4:g.186286441T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286441T>A , CM000666.2:g.186286441T>A	GRCh38
NC_000004.11:g.187207595T>A , CM000666.1:g.187207595T>A	GRCh37
NC_000004.10:g.187444589T>A	NCBI36
NG_008051.1:g.25478T>A , LRG_583:g.25478T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1507T>A (F11) MANE Select	ENSP00000384957.2:p.Ser503Thr
ENST00000264691.4:c.176+628T>A (F11)
ENST00000264692.8:c.1345T>A (F11)	ENSP00000264692.5:p.Ser449Thr
ENST00000403665.6:c.1507T>A (F11)	ENSP00000384957.2:p.Ser503Thr
NM_000128.3:c.1507T>A , LRG_583t1:c.1507T>A (F11)	NP_000119.1:p.Ser503Thr
NR_033900.1:n.1067-175A>T (F11-AS1)
XM_005262821.2:c.1510T>A (F11)	XP_005262878.1:p.Ser504Thr
XM_005262822.2:c.1483+628T>A (F11)	XP_005262879.1:n.1483+628T>A
XM_005262823.2:c.1240T>A (F11)	XP_005262880.1:p.Ser414Thr
XM_005262824.1:c.1484-105T>A (F11)	XP_005262881.1:n.1484-105T>A
XM_006714137.1:c.1462T>A (F11)	XP_006714200.1:p.Ser488Thr
XR_938706.1:n.1915T>A (F11)
XR_938707.1:n.1888+628T>A (F11)
XM_005262821.4:c.1510T>A (F11)	XP_005262878.1:p.Ser504Thr
XM_005262822.4:c.1483+628T>A (F11)	XP_005262879.1:n.1483+628T>A
XM_005262823.4:c.1240T>A (F11)	XP_005262880.1:p.Ser414Thr
XM_006714137.3:c.1462T>A (F11)	XP_006714200.1:p.Ser488Thr
XR_001741172.2:n.1981T>A (F11)
NM_000128.4:c.1507T>A (F11) MANE Select	NP_000119.1:p.Ser503Thr