Canonical Allele Identifier: CA2672904049
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI

Linked Data

gnomAD v4: 4-186288451-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186288454del , CM000666.2:g.186288454del GRCh38
NC_000004.11:g.187209608del , CM000666.1:g.187209608del GRCh37
NC_000004.10:g.187446602del NCBI36
NG_008051.1:g.27491del , LRG_583:g.27491del

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1718del (F11)
ENST00000264691.4:c.318del (F11)
ENST00000264692.8:c.1556del (F11)
ENST00000403665.6:c.1718del (F11)
ENST00000503841.1:n.237del (F11)
NM_000128.3:c.1718del , LRG_583t1:c.1718del (F11)
NR_033900.1:n.1042del (F11-AS1)
XM_005262821.2:c.1721del (F11)
XM_005262822.2:c.1625del (F11)
XM_005262823.2:c.1451del (F11)
XM_006714137.1:c.1673del (F11)
XM_005262821.4:c.1721del (F11)
XM_005262822.4:c.1625del (F11)
XM_005262823.4:c.1451del (F11)
XM_006714137.3:c.1673del (F11)
NM_000128.4:c.1718del (F11)
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