Canonical Allele Identifier: CA2672903868
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

gnomAD v4: 4-186287610-T-TATA
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287610_186287611insATA , CM000666.2:g.186287610_186287611insATA GRCh38
NC_000004.11:g.187208764_187208765insATA , CM000666.1:g.187208764_187208765insATA GRCh37
NC_000004.10:g.187445758_187445759insATA NCBI36
NG_008051.1:g.26647_26648insATA , LRG_583:g.26647_26648insATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1577-74_1577-73insATA (F11) MANE Select ENSP00000384957.2:n.1577-74_1577-73insATA
ENST00000264691.4:c.177-74_177-73insATA (F11)
ENST00000264692.8:c.1415-74_1415-73insATA (F11) ENSP00000264692.5:n.1415-74_1415-73insATA
ENST00000403665.6:c.1577-74_1577-73insATA (F11) ENSP00000384957.2:n.1577-74_1577-73insATA
ENST00000503841.1:n.22_23insATA (F11)
NM_000128.3:c.1577-74_1577-73insATA , LRG_583t1:c.1577-74_1577-73insATA (F11) NP_000119.1:n.1577-74_1577-73insATA
NR_033900.1:n.1066+817_1066+818insTAT (F11-AS1)
XM_005262821.2:c.1580-74_1580-73insATA (F11) XP_005262878.1:n.1580-74_1580-73insATA
XM_005262822.2:c.1484-74_1484-73insATA (F11) XP_005262879.1:n.1484-74_1484-73insATA
XM_005262823.2:c.1310-74_1310-73insATA (F11) XP_005262880.1:n.1310-74_1310-73insATA
XM_006714137.1:c.1532-74_1532-73insATA (F11) XP_006714200.1:n.1532-74_1532-73insATA
XR_938706.1:n.1985-74_1985-73insATA (F11)
XR_938707.1:n.1889-74_1889-73insATA (F11)
XM_005262821.4:c.1580-74_1580-73insATA (F11) XP_005262878.1:n.1580-74_1580-73insATA
XM_005262822.4:c.1484-74_1484-73insATA (F11) XP_005262879.1:n.1484-74_1484-73insATA
XM_005262823.4:c.1310-74_1310-73insATA (F11) XP_005262880.1:n.1310-74_1310-73insATA
XM_006714137.3:c.1532-74_1532-73insATA (F11) XP_006714200.1:n.1532-74_1532-73insATA
NM_000128.4:c.1577-74_1577-73insATA (F11) MANE Select NP_000119.1:n.1577-74_1577-73insATA
Search 100 bp 5'
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