Canonical Allele Identifier: CA219110
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 68177
ClinVar RCV Id: RCV000059009
dbSNP Id: rs281875242

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285775T>G , CM000666.2:g.186285775T>G GRCh38
NC_000004.11:g.187206929T>G , CM000666.1:g.187206929T>G GRCh37
NC_000004.10:g.187443923T>G NCBI36
NG_008051.1:g.24812T>G , LRG_583:g.24812T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1442T>G MANE Select ENSP00000384957.2:p.Ile481Ser
ENST00000264691.4:c.138T>G
ENST00000264692.8:c.1280T>G ENSP00000264692.5:p.Ile427Ser
ENST00000403665.6:c.1442T>G ENSP00000384957.2:p.Ile481Ser
NM_000128.3:c.1442T>G , LRG_583t1:c.1442T>G NP_000119.1:p.Ile481Ser
XM_005262821.2:c.1445T>G XP_005262878.1:p.Ile482Ser
XM_005262822.2:c.1445T>G XP_005262879.1:p.Ile482Ser
XM_005262823.2:c.1175T>G XP_005262880.1:p.Ile392Ser
XM_005262824.1:c.1445T>G XP_005262881.1:p.Ile482Ser
XM_006714137.1:c.1397T>G XP_006714200.1:p.Ile466Ser
XR_938706.1:n.1850T>G
XR_938707.1:n.1850T>G
XM_005262821.4:c.1445T>G XP_005262878.1:p.Ile482Ser
XM_005262822.4:c.1445T>G XP_005262879.1:p.Ile482Ser
XM_005262823.4:c.1175T>G XP_005262880.1:p.Ile392Ser
XM_006714137.3:c.1397T>G XP_006714200.1:p.Ile466Ser
XR_001741172.2:n.1916T>G
NM_000128.4:c.1442T>G MANE Select NP_000119.1:p.Ile481Ser