Canonical Allele Identifier: CA1071927461
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1741191954
gnomAD v3: 4-186286100-CTAAAGATAATTTAT-C
gnomAD v4: 4-186286100-CTAAAGATAATTTAT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186286114_186286127del , CM000666.2:g.186286114_186286127del GRCh38
NC_000004.11:g.187207268_187207281del , CM000666.1:g.187207268_187207281del GRCh37
NC_000004.10:g.187444262_187444275del NCBI36
NG_008051.1:g.25151_25164del , LRG_583:g.25151_25164del

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1481-301_1481-288del (F11) MANE Select ENSP00000384957.2:n.1481-301_1481-288del
ENST00000264691.4:c.176+301_176+314del (F11)
ENST00000264692.8:c.1319-301_1319-288del (F11) ENSP00000264692.5:n.1319-301_1319-288del
ENST00000403665.6:c.1481-301_1481-288del (F11) ENSP00000384957.2:n.1481-301_1481-288del
NM_000128.3:c.1481-301_1481-288del , LRG_583t1:c.1481-301_1481-288del (F11) NP_000119.1:n.1481-301_1481-288del
NR_033900.1:n.1219_1232del (F11-AS1)
XM_005262821.2:c.1484-301_1484-288del (F11) XP_005262878.1:n.1484-301_1484-288del
XM_005262822.2:c.1483+301_1483+314del (F11) XP_005262879.1:n.1483+301_1483+314del
XM_005262823.2:c.1214-301_1214-288del (F11) XP_005262880.1:n.1214-301_1214-288del
XM_005262824.1:c.1483+301_1483+314del (F11) XP_005262881.1:n.1483+301_1483+314del
XM_006714137.1:c.1436-301_1436-288del (F11) XP_006714200.1:n.1436-301_1436-288del
XR_938706.1:n.1889-301_1889-288del (F11)
XR_938707.1:n.1888+301_1888+314del (F11)
XM_005262821.4:c.1484-301_1484-288del (F11) XP_005262878.1:n.1484-301_1484-288del
XM_005262822.4:c.1483+301_1483+314del (F11) XP_005262879.1:n.1483+301_1483+314del
XM_005262823.4:c.1214-301_1214-288del (F11) XP_005262880.1:n.1214-301_1214-288del
XM_006714137.3:c.1436-301_1436-288del (F11) XP_006714200.1:n.1436-301_1436-288del
XR_001741172.2:n.1955-301_1955-288del (F11)
NM_000128.4:c.1481-301_1481-288del (F11) MANE Select NP_000119.1:n.1481-301_1481-288del
Search 100 bp 5'
Search 100 bp 3'