Canonical Allele Identifier: CA2672903836
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

gnomAD v4: 4-186287586-T-TTA
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287587_186287588dup , CM000666.2:g.186287587_186287588dup GRCh38
NC_000004.11:g.187208741_187208742dup , CM000666.1:g.187208741_187208742dup GRCh37
NC_000004.10:g.187445735_187445736dup NCBI36
NG_008051.1:g.26624_26625dup , LRG_583:g.26624_26625dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1577-97_1577-96dup (F11) MANE Select ENSP00000384957.2:n.1577-97_1577-96dup
ENST00000264691.4:c.177-97_177-96dup (F11)
ENST00000264692.8:c.1415-97_1415-96dup (F11) ENSP00000264692.5:n.1415-97_1415-96dup
ENST00000403665.6:c.1577-97_1577-96dup (F11) ENSP00000384957.2:n.1577-97_1577-96dup
NM_000128.3:c.1577-97_1577-96dup , LRG_583t1:c.1577-97_1577-96dup (F11) NP_000119.1:n.1577-97_1577-96dup
NR_033900.1:n.1066+840_1066+841dup (F11-AS1)
XM_005262821.2:c.1580-97_1580-96dup (F11) XP_005262878.1:n.1580-97_1580-96dup
XM_005262822.2:c.1484-97_1484-96dup (F11) XP_005262879.1:n.1484-97_1484-96dup
XM_005262823.2:c.1310-97_1310-96dup (F11) XP_005262880.1:n.1310-97_1310-96dup
XM_006714137.1:c.1532-97_1532-96dup (F11) XP_006714200.1:n.1532-97_1532-96dup
XR_938706.1:n.1985-97_1985-96dup (F11)
XR_938707.1:n.1889-97_1889-96dup (F11)
XM_005262821.4:c.1580-97_1580-96dup (F11) XP_005262878.1:n.1580-97_1580-96dup
XM_005262822.4:c.1484-97_1484-96dup (F11) XP_005262879.1:n.1484-97_1484-96dup
XM_005262823.4:c.1310-97_1310-96dup (F11) XP_005262880.1:n.1310-97_1310-96dup
XM_006714137.3:c.1532-97_1532-96dup (F11) XP_006714200.1:n.1532-97_1532-96dup
NM_000128.4:c.1577-97_1577-96dup (F11) MANE Select NP_000119.1:n.1577-97_1577-96dup
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