Canonical Allele Identifier: CA2672903830
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

gnomAD v4: 4-186287582-T-TCAG
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287584_186287585insGCA , CM000666.2:g.186287584_186287585insGCA GRCh38
NC_000004.11:g.187208738_187208739insGCA , CM000666.1:g.187208738_187208739insGCA GRCh37
NC_000004.10:g.187445732_187445733insGCA NCBI36
NG_008051.1:g.26621_26622insGCA , LRG_583:g.26621_26622insGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1577-100_1577-99insGCA (F11) MANE Select ENSP00000384957.2:n.1577-100_1577-99insGCA
ENST00000264691.4:c.177-100_177-99insGCA (F11)
ENST00000264692.8:c.1415-100_1415-99insGCA (F11) ENSP00000264692.5:n.1415-100_1415-99insGCA
ENST00000403665.6:c.1577-100_1577-99insGCA (F11) ENSP00000384957.2:n.1577-100_1577-99insGCA
NM_000128.3:c.1577-100_1577-99insGCA , LRG_583t1:c.1577-100_1577-99insGCA (F11) NP_000119.1:n.1577-100_1577-99insGCA
NR_033900.1:n.1066+845_1066+846insCTG (F11-AS1)
XM_005262821.2:c.1580-100_1580-99insGCA (F11) XP_005262878.1:n.1580-100_1580-99insGCA
XM_005262822.2:c.1484-100_1484-99insGCA (F11) XP_005262879.1:n.1484-100_1484-99insGCA
XM_005262823.2:c.1310-100_1310-99insGCA (F11) XP_005262880.1:n.1310-100_1310-99insGCA
XM_006714137.1:c.1532-100_1532-99insGCA (F11) XP_006714200.1:n.1532-100_1532-99insGCA
XR_938706.1:n.1985-100_1985-99insGCA (F11)
XR_938707.1:n.1889-100_1889-99insGCA (F11)
XM_005262821.4:c.1580-100_1580-99insGCA (F11) XP_005262878.1:n.1580-100_1580-99insGCA
XM_005262822.4:c.1484-100_1484-99insGCA (F11) XP_005262879.1:n.1484-100_1484-99insGCA
XM_005262823.4:c.1310-100_1310-99insGCA (F11) XP_005262880.1:n.1310-100_1310-99insGCA
XM_006714137.3:c.1532-100_1532-99insGCA (F11) XP_006714200.1:n.1532-100_1532-99insGCA
NM_000128.4:c.1577-100_1577-99insGCA (F11) MANE Select NP_000119.1:n.1577-100_1577-99insGCA
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