Canonical Allele Identifier: CA2982920970

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280237del , CM000666.2:g.186280237del	GRCh38
NC_000004.11:g.187201391del , CM000666.1:g.187201391del	GRCh37
NC_000004.10:g.187438385del	NCBI36
NG_008051.1:g.19274del , LRG_583:g.19274del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.880del MANE Select	ENSP00000384957.2:p.Ser294HisfsTer?
ENST00000264692.8:c.718del	ENSP00000264692.5:p.Ser240HisfsTer?
ENST00000403665.6:c.880del	ENSP00000384957.2:p.Ser294HisfsTer?
ENST00000452239.1:c.327del
NM_000128.3:c.880del , LRG_583t1:c.880del	NP_000119.1:p.Ser294HisfsTer?
XM_005262821.2:c.880del	XP_005262878.1:p.Ser294HisfsTer?
XM_005262822.2:c.880del	XP_005262879.1:p.Ser294HisfsTer?
XM_005262823.2:c.610del	XP_005262880.1:p.Ser204HisfsTer?
XM_005262824.1:c.880del	XP_005262881.1:p.Ser294HisfsTer?
XM_006714137.1:c.866-34del	XP_006714200.1:n.866-34del
XR_938706.1:n.1232del
XR_938707.1:n.1232del
XM_005262821.4:c.880del	XP_005262878.1:p.Ser294HisfsTer?
XM_005262822.4:c.880del	XP_005262879.1:p.Ser294HisfsTer?
XM_005262823.4:c.610del	XP_005262880.1:p.Ser204HisfsTer?
XM_006714137.3:c.866-34del	XP_006714200.1:n.866-34del
XM_017007884.2:c.880del	XP_016863373.1:p.Ser294HisfsTer?
XM_017007885.2:c.880del	XP_016863374.1:p.Ser294HisfsTer?
XM_017007886.2:c.880del	XP_016863375.1:p.Ser294HisfsTer?
XR_001741172.2:n.1213del
NM_000128.4:c.880del MANE Select	NP_000119.1:p.Ser294HisfsTer?