Canonical Allele Identifier: CA792348951
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1214493032

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186266987_186266991del , CM000666.2:g.186266987_186266991del GRCh38
NC_000004.11:g.187188141_187188145del , CM000666.1:g.187188141_187188145del GRCh37
NC_000004.10:g.187425135_187425139del NCBI36
NG_008051.1:g.6024_6028del , LRG_583:g.6024_6028del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.-1-149_-1-145del MANE Select ENSP00000384957.2:n.-1-149_-1-145del
ENST00000264692.8:c.-1-149_-1-145del ENSP00000264692.5:n.-1-149_-1-145del
ENST00000403665.6:c.-1-149_-1-145del ENSP00000384957.2:n.-1-149_-1-145del
ENST00000492972.6:c.-1-149_-1-145del ENSP00000424479.1:n.-1-149_-1-145del
NM_000128.3:c.-1-149_-1-145del , LRG_583t1:c.-1-149_-1-145del NP_000119.1:n.-1-149_-1-145del
XM_005262821.2:c.-1-149_-1-145del XP_005262878.1:n.-1-149_-1-145del
XM_005262822.2:c.-1-149_-1-145del XP_005262879.1:n.-1-149_-1-145del
XM_005262823.2:c.-1-149_-1-145del XP_005262880.1:n.-1-149_-1-145del
XM_005262824.1:c.-1-149_-1-145del XP_005262881.1:n.-1-149_-1-145del
XM_006714137.1:c.-1-149_-1-145del XP_006714200.1:n.-1-149_-1-145del
XR_938706.1:n.352-149_352-145del
XR_938707.1:n.352-149_352-145del
NM_001354804.1:c.-1-149_-1-145del NP_001341733.1:n.-1-149_-1-145del
XM_005262821.4:c.-1-149_-1-145del XP_005262878.1:n.-1-149_-1-145del
XM_005262822.4:c.-1-149_-1-145del XP_005262879.1:n.-1-149_-1-145del
XM_005262823.4:c.-1-149_-1-145del XP_005262880.1:n.-1-149_-1-145del
XM_006714137.3:c.-1-149_-1-145del XP_006714200.1:n.-1-149_-1-145del
XM_017007884.2:c.-1-149_-1-145del XP_016863373.1:n.-1-149_-1-145del
XM_017007885.2:c.-1-149_-1-145del XP_016863374.1:n.-1-149_-1-145del
XM_017007886.2:c.-1-149_-1-145del XP_016863375.1:n.-1-149_-1-145del
XR_001741172.2:n.333-149_333-145del
NM_000128.4:c.-1-149_-1-145del MANE Select NP_000119.1:n.-1-149_-1-145del
NM_001354804.2:c.-1-149_-1-145del NP_001341733.1:n.-1-149_-1-145del