Canonical Allele Identifier: CA891862598
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280319del , CM000666.2:g.186280319del GRCh38
NC_000004.11:g.187201473del , CM000666.1:g.187201473del GRCh37
NC_000004.10:g.187438467del NCBI36
NG_008051.1:g.19356del , LRG_583:g.19356del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.962del MANE Select ENSP00000384957.2:p.Cys321SerfsTer28
ENST00000264692.8:c.800del ENSP00000264692.5:p.Cys267SerfsTer28
ENST00000403665.6:c.962del ENSP00000384957.2:p.Cys321SerfsTer28
ENST00000452239.1:c.409del
NM_000128.3:c.962del , LRG_583t1:c.962del NP_000119.1:p.Cys321SerfsTer28
XM_005262821.2:c.962del XP_005262878.1:p.Cys321SerfsTer29
XM_005262822.2:c.962del XP_005262879.1:p.Cys321SerfsTer29
XM_005262823.2:c.692del XP_005262880.1:p.Cys231SerfsTer29
XM_005262824.1:c.962del XP_005262881.1:p.Cys321SerfsTer29
XM_006714137.1:c.914del XP_006714200.1:p.Cys305SerfsTer29
XR_938706.1:n.1314del
XR_938707.1:n.1314del
XM_005262821.4:c.962del XP_005262878.1:p.Cys321SerfsTer29
XM_005262822.4:c.962del XP_005262879.1:p.Cys321SerfsTer29
XM_005262823.4:c.692del XP_005262880.1:p.Cys231SerfsTer29
XM_006714137.3:c.914del XP_006714200.1:p.Cys305SerfsTer29
XM_017007884.2:c.962del XP_016863373.1:p.Cys321SerfsTer29
XM_017007885.2:c.962del XP_016863374.1:p.Cys321SerfsTer29
XM_017007886.2:c.962del XP_016863375.1:p.Cys321SerfsTer28
XR_001741172.2:n.1295del
NM_000128.4:c.962del MANE Select NP_000119.1:p.Cys321SerfsTer28