Canonical Allele Identifier: CA2672902990
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285771_186285777del , CM000666.2:g.186285771_186285777del GRCh38
NC_000004.11:g.187206925_187206931del , CM000666.1:g.187206925_187206931del GRCh37
NC_000004.10:g.187443919_187443925del NCBI36
NG_008051.1:g.24808_24814del , LRG_583:g.24808_24814del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1438_1444del MANE Select ENSP00000384957.2:p.Asp480ProfsTer3
ENST00000264691.4:c.134_140del
ENST00000264692.8:c.1276_1282del ENSP00000264692.5:p.Asp426ProfsTer3
ENST00000403665.6:c.1438_1444del ENSP00000384957.2:p.Asp480ProfsTer3
NM_000128.3:c.1438_1444del , LRG_583t1:c.1438_1444del NP_000119.1:p.Asp480ProfsTer3
XM_005262821.2:c.1441_1447del XP_005262878.1:p.Asp481ProfsTer3
XM_005262822.2:c.1441_1447del XP_005262879.1:p.Asp481ProfsTer3
XM_005262823.2:c.1171_1177del XP_005262880.1:p.Asp391ProfsTer3
XM_005262824.1:c.1441_1447del XP_005262881.1:p.Asp481ProfsTer3
XM_006714137.1:c.1393_1399del XP_006714200.1:p.Asp465ProfsTer3
XR_938706.1:n.1846_1852del
XR_938707.1:n.1846_1852del
XM_005262821.4:c.1441_1447del XP_005262878.1:p.Asp481ProfsTer3
XM_005262822.4:c.1441_1447del XP_005262879.1:p.Asp481ProfsTer3
XM_005262823.4:c.1171_1177del XP_005262880.1:p.Asp391ProfsTer3
XM_006714137.3:c.1393_1399del XP_006714200.1:p.Asp465ProfsTer3
XR_001741172.2:n.1912_1918del
NM_000128.4:c.1438_1444del MANE Select NP_000119.1:p.Asp480ProfsTer3