Canonical Allele Identifier: CA1071931960
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1739591447

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186267472_186267474del , CM000666.2:g.186267472_186267474del GRCh38
NC_000004.11:g.187188626_187188628del , CM000666.1:g.187188626_187188628del GRCh37
NC_000004.10:g.187425620_187425622del NCBI36
NG_008051.1:g.6509_6511del , LRG_583:g.6509_6511del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.55+281_55+283del MANE Select ENSP00000384957.2:n.55+281_55+283del
ENST00000264692.8:c.55+281_55+283del ENSP00000264692.5:n.55+281_55+283del
ENST00000403665.6:c.55+281_55+283del ENSP00000384957.2:n.55+281_55+283del
ENST00000492972.6:c.55+281_55+283del ENSP00000424479.1:n.55+281_55+283del
NM_000128.3:c.55+281_55+283del , LRG_583t1:c.55+281_55+283del NP_000119.1:n.55+281_55+283del
XM_005262821.2:c.55+281_55+283del XP_005262878.1:n.55+281_55+283del
XM_005262822.2:c.55+281_55+283del XP_005262879.1:n.55+281_55+283del
XM_005262823.2:c.55+281_55+283del XP_005262880.1:n.55+281_55+283del
XM_005262824.1:c.55+281_55+283del XP_005262881.1:n.55+281_55+283del
XM_006714137.1:c.55+281_55+283del XP_006714200.1:n.55+281_55+283del
XR_938706.1:n.407+281_407+283del
XR_938707.1:n.407+281_407+283del
NM_001354804.1:c.55+281_55+283del NP_001341733.1:n.55+281_55+283del
XM_005262821.4:c.55+281_55+283del XP_005262878.1:n.55+281_55+283del
XM_005262822.4:c.55+281_55+283del XP_005262879.1:n.55+281_55+283del
XM_005262823.4:c.55+281_55+283del XP_005262880.1:n.55+281_55+283del
XM_006714137.3:c.55+281_55+283del XP_006714200.1:n.55+281_55+283del
XM_017007884.2:c.55+281_55+283del XP_016863373.1:n.55+281_55+283del
XM_017007885.2:c.55+281_55+283del XP_016863374.1:n.55+281_55+283del
XM_017007886.2:c.55+281_55+283del XP_016863375.1:n.55+281_55+283del
XR_001741172.2:n.388+281_388+283del
NM_000128.4:c.55+281_55+283del MANE Select NP_000119.1:n.55+281_55+283del
NM_001354804.2:c.55+281_55+283del NP_001341733.1:n.55+281_55+283del