Canonical Allele Identifier: CA2672903847
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

gnomAD v4: 4-186287594-ATAT-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287595_186287597del , CM000666.2:g.186287595_186287597del GRCh38
NC_000004.11:g.187208749_187208751del , CM000666.1:g.187208749_187208751del GRCh37
NC_000004.10:g.187445743_187445745del NCBI36
NG_008051.1:g.26632_26634del , LRG_583:g.26632_26634del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1577-89_1577-87del (F11) MANE Select ENSP00000384957.2:n.1577-89_1577-87del
ENST00000264691.4:c.177-89_177-87del (F11)
ENST00000264692.8:c.1415-89_1415-87del (F11) ENSP00000264692.5:n.1415-89_1415-87del
ENST00000403665.6:c.1577-89_1577-87del (F11) ENSP00000384957.2:n.1577-89_1577-87del
ENST00000503841.1:n.7_9del (F11)
NM_000128.3:c.1577-89_1577-87del , LRG_583t1:c.1577-89_1577-87del (F11) NP_000119.1:n.1577-89_1577-87del
NR_033900.1:n.1066+831_1066+833del (F11-AS1)
XM_005262821.2:c.1580-89_1580-87del (F11) XP_005262878.1:n.1580-89_1580-87del
XM_005262822.2:c.1484-89_1484-87del (F11) XP_005262879.1:n.1484-89_1484-87del
XM_005262823.2:c.1310-89_1310-87del (F11) XP_005262880.1:n.1310-89_1310-87del
XM_006714137.1:c.1532-89_1532-87del (F11) XP_006714200.1:n.1532-89_1532-87del
XR_938706.1:n.1985-89_1985-87del (F11)
XR_938707.1:n.1889-89_1889-87del (F11)
XM_005262821.4:c.1580-89_1580-87del (F11) XP_005262878.1:n.1580-89_1580-87del
XM_005262822.4:c.1484-89_1484-87del (F11) XP_005262879.1:n.1484-89_1484-87del
XM_005262823.4:c.1310-89_1310-87del (F11) XP_005262880.1:n.1310-89_1310-87del
XM_006714137.3:c.1532-89_1532-87del (F11) XP_006714200.1:n.1532-89_1532-87del
NM_000128.4:c.1577-89_1577-87del (F11) MANE Select NP_000119.1:n.1577-89_1577-87del
Search 100 bp 5'
Search 100 bp 3'