Canonical Allele Identifier: CA2672903907

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186287822-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287824del , CM000666.2:g.186287824del	GRCh38
NC_000004.11:g.187208978del , CM000666.1:g.187208978del	GRCh37
NC_000004.10:g.187445972del	NCBI36
NG_008051.1:g.26861del , LRG_583:g.26861del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+1del (F11)
ENST00000264691.4:c.316+1del (F11)
ENST00000264692.8:c.1554+1del (F11)
ENST00000403665.6:c.1716+1del (F11)
ENST00000503841.1:n.235+1del (F11)
NM_000128.3:c.1716+1del , LRG_583t1:c.1716+1del (F11)
NR_033900.1:n.1066+605del (F11-AS1)
XM_005262821.2:c.1719+1del (F11)
XM_005262822.2:c.1623+1del (F11)
XM_005262823.2:c.1449+1del (F11)
XM_006714137.1:c.1671+1del (F11)
XM_005262821.4:c.1719+1del (F11)
XM_005262822.4:c.1623+1del (F11)
XM_005262823.4:c.1449+1del (F11)
XM_006714137.3:c.1671+1del (F11)
NM_000128.4:c.1716+1del (F11)