Canonical Allele Identifier: CA917387472
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1009731279

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186274645_186274648dup , CM000666.2:g.186274645_186274648dup GRCh38
NC_000004.11:g.187195799_187195802dup , CM000666.1:g.187195799_187195802dup GRCh37
NC_000004.10:g.187432793_187432796dup NCBI36
NG_008051.1:g.13682_13685dup , LRG_583:g.13682_13685dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.485+370_485+373dup MANE Select ENSP00000384957.2:n.485+370_485+373dup
ENST00000264692.8:c.324-1142_324-1139dup ENSP00000264692.5:n.324-1142_324-1139dup
ENST00000403665.6:c.485+370_485+373dup ENSP00000384957.2:n.485+370_485+373dup
ENST00000492972.6:c.*366_*369dup ENSP00000424479.1:n.*366_*369dup
NM_000128.3:c.485+370_485+373dup , LRG_583t1:c.485+370_485+373dup NP_000119.1:n.485+370_485+373dup
XM_005262821.2:c.485+370_485+373dup XP_005262878.1:n.485+370_485+373dup
XM_005262822.2:c.485+370_485+373dup XP_005262879.1:n.485+370_485+373dup
XM_005262823.2:c.485+370_485+373dup XP_005262880.1:n.485+370_485+373dup
XM_005262824.1:c.485+370_485+373dup XP_005262881.1:n.485+370_485+373dup
XM_006714137.1:c.485+370_485+373dup XP_006714200.1:n.485+370_485+373dup
XR_938706.1:n.837+370_837+373dup
XR_938707.1:n.837+370_837+373dup
NM_001354804.1:c.*366_*369dup NP_001341733.1:n.*366_*369dup
XM_005262821.4:c.485+370_485+373dup XP_005262878.1:n.485+370_485+373dup
XM_005262822.4:c.485+370_485+373dup XP_005262879.1:n.485+370_485+373dup
XM_005262823.4:c.485+370_485+373dup XP_005262880.1:n.485+370_485+373dup
XM_006714137.3:c.485+370_485+373dup XP_006714200.1:n.485+370_485+373dup
XM_017007884.2:c.485+370_485+373dup XP_016863373.1:n.485+370_485+373dup
XM_017007885.2:c.485+370_485+373dup XP_016863374.1:n.485+370_485+373dup
XM_017007886.2:c.485+370_485+373dup XP_016863375.1:n.485+370_485+373dup
XR_001741172.2:n.818+370_818+373dup
NM_000128.4:c.485+370_485+373dup MANE Select NP_000119.1:n.485+370_485+373dup
NM_001354804.2:c.*366_*369dup NP_001341733.1:n.*366_*369dup