Canonical Allele Identifier: CA2672903855
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

gnomAD v4: 4-186287599-T-TATATATATATTTATATGTATGC
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287606_186287627dup , CM000666.2:g.186287606_186287627dup GRCh38
NC_000004.11:g.187208760_187208781dup , CM000666.1:g.187208760_187208781dup GRCh37
NC_000004.10:g.187445754_187445775dup NCBI36
NG_008051.1:g.26643_26664dup , LRG_583:g.26643_26664dup

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1577-78_1577-57dup (F11) MANE Select ENSP00000384957.2:n.1577-78_1577-57dup
ENST00000264691.4:c.177-78_177-57dup (F11)
ENST00000264692.8:c.1415-78_1415-57dup (F11) ENSP00000264692.5:n.1415-78_1415-57dup
ENST00000403665.6:c.1577-78_1577-57dup (F11) ENSP00000384957.2:n.1577-78_1577-57dup
ENST00000503841.1:n.18_39dup (F11)
NM_000128.3:c.1577-78_1577-57dup , LRG_583t1:c.1577-78_1577-57dup (F11) NP_000119.1:n.1577-78_1577-57dup
NR_033900.1:n.1066+807_1066+828dup (F11-AS1)
XM_005262821.2:c.1580-78_1580-57dup (F11) XP_005262878.1:n.1580-78_1580-57dup
XM_005262822.2:c.1484-78_1484-57dup (F11) XP_005262879.1:n.1484-78_1484-57dup
XM_005262823.2:c.1310-78_1310-57dup (F11) XP_005262880.1:n.1310-78_1310-57dup
XM_006714137.1:c.1532-78_1532-57dup (F11) XP_006714200.1:n.1532-78_1532-57dup
XR_938706.1:n.1985-78_1985-57dup (F11)
XR_938707.1:n.1889-78_1889-57dup (F11)
XM_005262821.4:c.1580-78_1580-57dup (F11) XP_005262878.1:n.1580-78_1580-57dup
XM_005262822.4:c.1484-78_1484-57dup (F11) XP_005262879.1:n.1484-78_1484-57dup
XM_005262823.4:c.1310-78_1310-57dup (F11) XP_005262880.1:n.1310-78_1310-57dup
XM_006714137.3:c.1532-78_1532-57dup (F11) XP_006714200.1:n.1532-78_1532-57dup
NM_000128.4:c.1577-78_1577-57dup (F11) MANE Select NP_000119.1:n.1577-78_1577-57dup
Search 100 bp 5'
Search 100 bp 3'