Canonical Allele Identifier: CA121752
Gene: F11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11896
ClinVar RCV Id: RCV000012671
dbSNP Id: rs121965066

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186274228C>A , CM000666.2:g.186274228C>A GRCh38
NC_000004.11:g.187195382C>A , CM000666.1:g.187195382C>A GRCh37
NC_000004.10:g.187432376C>A NCBI36
NG_008051.1:g.13265C>A , LRG_583:g.13265C>A

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.438C>A , LRG_583t1:c.438C>A NP_000119.1:p.Cys146Ter
XM_005262821.2:c.438C>A XP_005262878.1:p.Cys146Ter
XM_005262822.2:c.438C>A XP_005262879.1:p.Cys146Ter
XM_005262823.2:c.438C>A XP_005262880.1:p.Cys146Ter
XM_005262824.1:c.438C>A XP_005262881.1:p.Cys146Ter
XM_006714137.1:c.438C>A XP_006714200.1:p.Cys146Ter
XR_938706.1:n.790C>A
XR_938707.1:n.790C>A
NM_001354804.1:c.438C>A VV NP_001341733.1:p.Cys146Ter
XM_005262821.4:c.438C>A XP_005262878.1:p.Cys146Ter
XM_005262822.4:c.438C>A XP_005262879.1:p.Cys146Ter
XM_005262823.4:c.438C>A XP_005262880.1:p.Cys146Ter
XM_006714137.3:c.438C>A XP_006714200.1:p.Cys146Ter
XM_017007884.2:c.438C>A XP_016863373.1:p.Cys146Ter
XM_017007885.2:c.438C>A XP_016863374.1:p.Cys146Ter
XM_017007886.2:c.438C>A XP_016863375.1:p.Cys146Ter
XR_001741172.2:n.771C>A
ENST00000264692.8:c.323+1053C>A ENSP00000264692.5:p.=
ENST00000403665.6:c.438C>A ENSP00000384957.2:p.Cys146Ter
ENST00000492972.6:c.438C>A ENSP00000424479.1:p.Cys146Ter
ENST00000514715.1:n.310C>A