Canonical Allele Identifier: CA2672902482
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280378del , CM000666.2:g.186280378del GRCh38
NC_000004.11:g.187201532del , CM000666.1:g.187201532del GRCh37
NC_000004.10:g.187438526del NCBI36
NG_008051.1:g.19415del , LRG_583:g.19415del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1021del MANE Select ENSP00000384957.2:p.Glu341LysfsTer8
ENST00000264692.8:c.859del ENSP00000264692.5:p.Glu287LysfsTer8
ENST00000403665.6:c.1021del ENSP00000384957.2:p.Glu341LysfsTer8
ENST00000452239.1:c.468del
NM_000128.3:c.1021del , LRG_583t1:c.1021del NP_000119.1:p.Glu341LysfsTer8
XM_005262821.2:c.1021del XP_005262878.1:p.Glu341LysfsTer9
XM_005262822.2:c.1021del XP_005262879.1:p.Glu341LysfsTer9
XM_005262823.2:c.751del XP_005262880.1:p.Glu251LysfsTer9
XM_005262824.1:c.1021del XP_005262881.1:p.Glu341LysfsTer9
XM_006714137.1:c.973del XP_006714200.1:p.Glu325LysfsTer9
XR_938706.1:n.1373del
XR_938707.1:n.1373del
XM_005262821.4:c.1021del XP_005262878.1:p.Glu341LysfsTer9
XM_005262822.4:c.1021del XP_005262879.1:p.Glu341LysfsTer9
XM_005262823.4:c.751del XP_005262880.1:p.Glu251LysfsTer9
XM_006714137.3:c.973del XP_006714200.1:p.Glu325LysfsTer9
XM_017007884.2:c.1021del XP_016863373.1:p.Glu341LysfsTer9
XM_017007885.2:c.1021del XP_016863374.1:p.Glu341LysfsTer9
XM_017007886.2:c.1021del XP_016863375.1:p.Glu341LysfsTer8
XR_001741172.2:n.1354del
NM_000128.4:c.1021del MANE Select NP_000119.1:p.Glu341LysfsTer8