Canonical Allele Identifier: CA2672902495
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284249_186284250del , CM000666.2:g.186284249_186284250del GRCh38
NC_000004.11:g.187205403_187205404del , CM000666.1:g.187205403_187205404del GRCh37
NC_000004.10:g.187442397_187442398del NCBI36
NG_008051.1:g.23286_23287del , LRG_583:g.23286_23287del

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1293_1294del MANE Select ENSP00000384957.2:p.His431GlnfsTer9
ENST00000264692.8:c.1131_1132del ENSP00000264692.5:p.His377GlnfsTer9
ENST00000403665.6:c.1293_1294del ENSP00000384957.2:p.His431GlnfsTer9
NM_000128.3:c.1293_1294del , LRG_583t1:c.1293_1294del NP_000119.1:p.His431GlnfsTer9
XM_005262821.2:c.1296_1297del XP_005262878.1:p.His432GlnfsTer9
XM_005262822.2:c.1296_1297del XP_005262879.1:p.His432GlnfsTer9
XM_005262823.2:c.1026_1027del XP_005262880.1:p.His342GlnfsTer9
XM_005262824.1:c.1296_1297del XP_005262881.1:p.His432GlnfsTer9
XM_006714137.1:c.1248_1249del XP_006714200.1:p.His416GlnfsTer9
XR_938706.1:n.1701_1702del
XR_938707.1:n.1701_1702del
XM_005262821.4:c.1296_1297del XP_005262878.1:p.His432GlnfsTer9
XM_005262822.4:c.1296_1297del XP_005262879.1:p.His432GlnfsTer9
XM_005262823.4:c.1026_1027del XP_005262880.1:p.His342GlnfsTer9
XM_006714137.3:c.1248_1249del XP_006714200.1:p.His416GlnfsTer9
XR_001741172.2:n.1767_1768del
NM_000128.4:c.1293_1294del MANE Select NP_000119.1:p.His431GlnfsTer9