Canonical Allele Identifier: CA1071933589
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1740090133

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186272981_186272983del , CM000666.2:g.186272981_186272983del GRCh38
NC_000004.11:g.187194135_187194137del , CM000666.1:g.187194135_187194137del GRCh37
NC_000004.10:g.187431129_187431131del NCBI36
NG_008051.1:g.12018_12020del , LRG_583:g.12018_12020del

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.219-90_219-88del MANE Select ENSP00000384957.2:n.219-90_219-88del
ENST00000264692.8:c.219-90_219-88del ENSP00000264692.5:n.219-90_219-88del
ENST00000403665.6:c.219-90_219-88del ENSP00000384957.2:n.219-90_219-88del
ENST00000492972.6:c.219-90_219-88del ENSP00000424479.1:n.219-90_219-88del
NM_000128.3:c.219-90_219-88del , LRG_583t1:c.219-90_219-88del NP_000119.1:n.219-90_219-88del
XM_005262821.2:c.219-90_219-88del XP_005262878.1:n.219-90_219-88del
XM_005262822.2:c.219-90_219-88del XP_005262879.1:n.219-90_219-88del
XM_005262823.2:c.219-90_219-88del XP_005262880.1:n.219-90_219-88del
XM_005262824.1:c.219-90_219-88del XP_005262881.1:n.219-90_219-88del
XM_006714137.1:c.219-90_219-88del XP_006714200.1:n.219-90_219-88del
XR_938706.1:n.571-90_571-88del
XR_938707.1:n.571-90_571-88del
NM_001354804.1:c.219-90_219-88del NP_001341733.1:n.219-90_219-88del
XM_005262821.4:c.219-90_219-88del XP_005262878.1:n.219-90_219-88del
XM_005262822.4:c.219-90_219-88del XP_005262879.1:n.219-90_219-88del
XM_005262823.4:c.219-90_219-88del XP_005262880.1:n.219-90_219-88del
XM_006714137.3:c.219-90_219-88del XP_006714200.1:n.219-90_219-88del
XM_017007884.2:c.219-90_219-88del XP_016863373.1:n.219-90_219-88del
XM_017007885.2:c.219-90_219-88del XP_016863374.1:n.219-90_219-88del
XM_017007886.2:c.219-90_219-88del XP_016863375.1:n.219-90_219-88del
XR_001741172.2:n.552-90_552-88del
NM_000128.4:c.219-90_219-88del MANE Select NP_000119.1:n.219-90_219-88del
NM_001354804.2:c.219-90_219-88del NP_001341733.1:n.219-90_219-88del