Canonical Allele Identifier: CA1071927785
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1554083992
gnomAD v3: 4-186287591-A-AT
gnomAD v4: 4-186287591-A-AT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287591_186287592insT , CM000666.2:g.186287591_186287592insT GRCh38
NC_000004.11:g.187208745_187208746insT , CM000666.1:g.187208745_187208746insT GRCh37
NC_000004.10:g.187445739_187445740insT NCBI36
NG_008051.1:g.26628_26629insT , LRG_583:g.26628_26629insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1577-93_1577-92insT (F11) MANE Select ENSP00000384957.2:n.1577-93_1577-92insT
ENST00000264691.4:c.177-93_177-92insT (F11)
ENST00000264692.8:c.1415-93_1415-92insT (F11) ENSP00000264692.5:n.1415-93_1415-92insT
ENST00000403665.6:c.1577-93_1577-92insT (F11) ENSP00000384957.2:n.1577-93_1577-92insT
ENST00000503841.1:n.3_4insT (F11)
NM_000128.3:c.1577-93_1577-92insT , LRG_583t1:c.1577-93_1577-92insT (F11) NP_000119.1:n.1577-93_1577-92insT
NR_033900.1:n.1066+836_1066+837insA (F11-AS1)
XM_005262821.2:c.1580-93_1580-92insT (F11) XP_005262878.1:n.1580-93_1580-92insT
XM_005262822.2:c.1484-93_1484-92insT (F11) XP_005262879.1:n.1484-93_1484-92insT
XM_005262823.2:c.1310-93_1310-92insT (F11) XP_005262880.1:n.1310-93_1310-92insT
XM_006714137.1:c.1532-93_1532-92insT (F11) XP_006714200.1:n.1532-93_1532-92insT
XR_938706.1:n.1985-93_1985-92insT (F11)
XR_938707.1:n.1889-93_1889-92insT (F11)
XM_005262821.4:c.1580-93_1580-92insT (F11) XP_005262878.1:n.1580-93_1580-92insT
XM_005262822.4:c.1484-93_1484-92insT (F11) XP_005262879.1:n.1484-93_1484-92insT
XM_005262823.4:c.1310-93_1310-92insT (F11) XP_005262880.1:n.1310-93_1310-92insT
XM_006714137.3:c.1532-93_1532-92insT (F11) XP_006714200.1:n.1532-93_1532-92insT
NM_000128.4:c.1577-93_1577-92insT (F11) MANE Select NP_000119.1:n.1577-93_1577-92insT
Search 100 bp 5'
Search 100 bp 3'