Canonical Allele Identifier: CA2764876457

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280243del , CM000666.2:g.186280243del	GRCh38
NC_000004.11:g.187201397del , CM000666.1:g.187201397del	GRCh37
NC_000004.10:g.187438391del	NCBI36
NG_008051.1:g.19280del , LRG_583:g.19280del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.886del MANE Select	ENSP00000384957.2:p.Tyr296ThrfsTer?
ENST00000264692.8:c.724del	ENSP00000264692.5:p.Tyr242ThrfsTer?
ENST00000403665.6:c.886del	ENSP00000384957.2:p.Tyr296ThrfsTer?
ENST00000452239.1:c.333del
NM_000128.3:c.886del , LRG_583t1:c.886del	NP_000119.1:p.Tyr296ThrfsTer?
XM_005262821.2:c.886del	XP_005262878.1:p.Tyr296ThrfsTer?
XM_005262822.2:c.886del	XP_005262879.1:p.Tyr296ThrfsTer?
XM_005262823.2:c.616del	XP_005262880.1:p.Tyr206ThrfsTer?
XM_005262824.1:c.886del	XP_005262881.1:p.Tyr296ThrfsTer?
XM_006714137.1:c.866-28del	XP_006714200.1:n.866-28del
XR_938706.1:n.1238del
XR_938707.1:n.1238del
XM_005262821.4:c.886del	XP_005262878.1:p.Tyr296ThrfsTer?
XM_005262822.4:c.886del	XP_005262879.1:p.Tyr296ThrfsTer?
XM_005262823.4:c.616del	XP_005262880.1:p.Tyr206ThrfsTer?
XM_006714137.3:c.866-28del	XP_006714200.1:n.866-28del
XM_017007884.2:c.886del	XP_016863373.1:p.Tyr296ThrfsTer?
XM_017007885.2:c.886del	XP_016863374.1:p.Tyr296ThrfsTer?
XM_017007886.2:c.886del	XP_016863375.1:p.Tyr296ThrfsTer?
XR_001741172.2:n.1219del
NM_000128.4:c.886del MANE Select	NP_000119.1:p.Tyr296ThrfsTer?