Canonical Allele Identifier: CA913103786

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187197429_187197435del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276276_186276282del , CM000666.2:g.186276276_186276282del	GRCh38
NC_000004.11:g.187197430_187197436del , CM000666.1:g.187197430_187197436del	GRCh37
NC_000004.10:g.187434424_187434430del	NCBI36
NG_008051.1:g.15313_15319del , LRG_583:g.15313_15319del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.641_647del MANE Select	ENSP00000384957.2:p.Asn214ThrfsTer?
ENST00000264692.8:c.479_485del	ENSP00000264692.5:p.Asn160ThrfsTer?
ENST00000403665.6:c.641_647del	ENSP00000384957.2:p.Asn214ThrfsTer?
ENST00000452239.1:c.88_94del
NM_000128.3:c.641_647del , LRG_583t1:c.641_647del	NP_000119.1:p.Asn214ThrfsTer?
XM_005262821.2:c.641_647del	XP_005262878.1:p.Asn214ThrfsTer?
XM_005262822.2:c.641_647del	XP_005262879.1:p.Asn214ThrfsTer?
XM_005262823.2:c.485+2001_485+2007del	XP_005262880.1:n.485+2001_485+2007del
XM_005262824.1:c.641_647del	XP_005262881.1:p.Asn214ThrfsTer?
XM_006714137.1:c.641_647del	XP_006714200.1:p.Asn214ThrfsTer?
XR_938706.1:n.993_999del
XR_938707.1:n.993_999del
XM_005262821.4:c.641_647del	XP_005262878.1:p.Asn214ThrfsTer?
XM_005262822.4:c.641_647del	XP_005262879.1:p.Asn214ThrfsTer?
XM_005262823.4:c.485+2001_485+2007del	XP_005262880.1:n.485+2001_485+2007del
XM_006714137.3:c.641_647del	XP_006714200.1:p.Asn214ThrfsTer?
XM_017007884.2:c.641_647del	XP_016863373.1:p.Asn214ThrfsTer?
XM_017007885.2:c.641_647del	XP_016863374.1:p.Asn214ThrfsTer?
XM_017007886.2:c.641_647del	XP_016863375.1:p.Asn214ThrfsTer?
XR_001741172.2:n.974_980del
NM_000128.4:c.641_647del MANE Select	NP_000119.1:p.Asn214ThrfsTer?