Canonical Allele Identifier: CA2695204111
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287821_186287834del , CM000666.2:g.186287821_186287834del GRCh38
NC_000004.11:g.187208975_187208988del , CM000666.1:g.187208975_187208988del GRCh37
NC_000004.10:g.187445969_187445982del NCBI36
NG_008051.1:g.26858_26871del , LRG_583:g.26858_26871del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1714_1716+11del (F11)
ENST00000264691.4:c.314_316+11del (F11)
ENST00000264692.8:c.1552_1554+11del (F11)
ENST00000403665.6:c.1714_1716+11del (F11)
ENST00000503841.1:n.233_235+11del (F11)
NM_000128.3:c.1714_1716+11del , LRG_583t1:c.1714_1716+11del (F11)
NR_033900.1:n.1066+594_1066+607del (F11-AS1)
XM_005262821.2:c.1717_1719+11del (F11)
XM_005262822.2:c.1621_1623+11del (F11)
XM_005262823.2:c.1447_1449+11del (F11)
XM_006714137.1:c.1669_1671+11del (F11)
XM_005262821.4:c.1717_1719+11del (F11)
XM_005262822.4:c.1621_1623+11del (F11)
XM_005262823.4:c.1447_1449+11del (F11)
XM_006714137.3:c.1669_1671+11del (F11)
NM_000128.4:c.1714_1716+11del (F11)
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