Canonical Allele Identifier: CA112105274
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1491205113
gnomAD v3: 4-186287592-A-ATG
gnomAD v4: 4-186287592-A-ATG
MyVariant Identifiers: chr4:g.187208746_187208747insTG (hg19) chr4:g.186287592_186287593insTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287593_186287594insGT , CM000666.2:g.186287593_186287594insGT GRCh38
NC_000004.11:g.187208747_187208748insGT , CM000666.1:g.187208747_187208748insGT GRCh37
NC_000004.10:g.187445741_187445742insGT NCBI36
NG_008051.1:g.26630_26631insGT , LRG_583:g.26630_26631insGT

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1577-91_1577-90insGT (F11) MANE Select ENSP00000384957.2:n.1577-91_1577-90insGT
ENST00000264691.4:c.177-91_177-90insGT (F11)
ENST00000264692.8:c.1415-91_1415-90insGT (F11) ENSP00000264692.5:n.1415-91_1415-90insGT
ENST00000403665.6:c.1577-91_1577-90insGT (F11) ENSP00000384957.2:n.1577-91_1577-90insGT
ENST00000503841.1:n.5_6insGT (F11)
NM_000128.3:c.1577-91_1577-90insGT , LRG_583t1:c.1577-91_1577-90insGT (F11) NP_000119.1:n.1577-91_1577-90insGT
NR_033900.1:n.1066+835_1066+836insCA (F11-AS1)
XM_005262821.2:c.1580-91_1580-90insGT (F11) XP_005262878.1:n.1580-91_1580-90insGT
XM_005262822.2:c.1484-91_1484-90insGT (F11) XP_005262879.1:n.1484-91_1484-90insGT
XM_005262823.2:c.1310-91_1310-90insGT (F11) XP_005262880.1:n.1310-91_1310-90insGT
XM_006714137.1:c.1532-91_1532-90insGT (F11) XP_006714200.1:n.1532-91_1532-90insGT
XR_938706.1:n.1985-91_1985-90insGT (F11)
XR_938707.1:n.1889-91_1889-90insGT (F11)
XM_005262821.4:c.1580-91_1580-90insGT (F11) XP_005262878.1:n.1580-91_1580-90insGT
XM_005262822.4:c.1484-91_1484-90insGT (F11) XP_005262879.1:n.1484-91_1484-90insGT
XM_005262823.4:c.1310-91_1310-90insGT (F11) XP_005262880.1:n.1310-91_1310-90insGT
XM_006714137.3:c.1532-91_1532-90insGT (F11) XP_006714200.1:n.1532-91_1532-90insGT
NM_000128.4:c.1577-91_1577-90insGT (F11) MANE Select NP_000119.1:n.1577-91_1577-90insGT
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