Canonical Allele Identifier: CA1519934212
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1192998631

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276352del , CM000666.2:g.186276352del GRCh38
NC_000004.11:g.187197506del , CM000666.1:g.187197506del GRCh37
NC_000004.10:g.187434500del NCBI36
NG_008051.1:g.15389del , LRG_583:g.15389del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.717del MANE Select ENSP00000384957.2:p.Phe239LeufsTer?
ENST00000264692.8:c.555del ENSP00000264692.5:p.Phe185LeufsTer?
ENST00000403665.6:c.717del ENSP00000384957.2:p.Phe239LeufsTer?
ENST00000452239.1:c.164del
NM_000128.3:c.717del , LRG_583t1:c.717del NP_000119.1:p.Phe239LeufsTer?
XM_005262821.2:c.717del XP_005262878.1:p.Phe239LeufsTer?
XM_005262822.2:c.717del XP_005262879.1:p.Phe239LeufsTer?
XM_005262823.2:c.485+2077del XP_005262880.1:n.485+2077del
XM_005262824.1:c.717del XP_005262881.1:p.Phe239LeufsTer?
XM_006714137.1:c.717del XP_006714200.1:p.Phe239LeufsTer?
XR_938706.1:n.1069del
XR_938707.1:n.1069del
XM_005262821.4:c.717del XP_005262878.1:p.Phe239LeufsTer?
XM_005262822.4:c.717del XP_005262879.1:p.Phe239LeufsTer?
XM_005262823.4:c.485+2077del XP_005262880.1:n.485+2077del
XM_006714137.3:c.717del XP_006714200.1:p.Phe239LeufsTer?
XM_017007884.2:c.717del XP_016863373.1:p.Phe239LeufsTer?
XM_017007885.2:c.717del XP_016863374.1:p.Phe239LeufsTer?
XM_017007886.2:c.717del XP_016863375.1:p.Phe239LeufsTer?
XR_001741172.2:n.1050del
NM_000128.4:c.717del MANE Select NP_000119.1:p.Phe239LeufsTer?