Canonical Allele Identifier: CA2672901560
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186274056_186274079del , CM000666.2:g.186274056_186274079del GRCh38
NC_000004.11:g.187195210_187195233del , CM000666.1:g.187195210_187195233del GRCh37
NC_000004.10:g.187432204_187432227del NCBI36
NG_008051.1:g.13093_13116del , LRG_583:g.13093_13116del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.326-60_326-37del MANE Select ENSP00000384957.2:n.326-60_326-37del
ENST00000264692.8:c.323+881_323+904del ENSP00000264692.5:n.323+881_323+904del
ENST00000403665.6:c.326-60_326-37del ENSP00000384957.2:n.326-60_326-37del
ENST00000492972.6:c.326-60_326-37del ENSP00000424479.1:n.326-60_326-37del
ENST00000514715.1:n.198-60_198-37del
NM_000128.3:c.326-60_326-37del , LRG_583t1:c.326-60_326-37del NP_000119.1:n.326-60_326-37del
XM_005262821.2:c.326-60_326-37del XP_005262878.1:n.326-60_326-37del
XM_005262822.2:c.326-60_326-37del XP_005262879.1:n.326-60_326-37del
XM_005262823.2:c.326-60_326-37del XP_005262880.1:n.326-60_326-37del
XM_005262824.1:c.326-60_326-37del XP_005262881.1:n.326-60_326-37del
XM_006714137.1:c.326-60_326-37del XP_006714200.1:n.326-60_326-37del
XR_938706.1:n.678-60_678-37del
XR_938707.1:n.678-60_678-37del
NM_001354804.1:c.326-60_326-37del NP_001341733.1:n.326-60_326-37del
XM_005262821.4:c.326-60_326-37del XP_005262878.1:n.326-60_326-37del
XM_005262822.4:c.326-60_326-37del XP_005262879.1:n.326-60_326-37del
XM_005262823.4:c.326-60_326-37del XP_005262880.1:n.326-60_326-37del
XM_006714137.3:c.326-60_326-37del XP_006714200.1:n.326-60_326-37del
XM_017007884.2:c.326-60_326-37del XP_016863373.1:n.326-60_326-37del
XM_017007885.2:c.326-60_326-37del XP_016863374.1:n.326-60_326-37del
XM_017007886.2:c.326-60_326-37del XP_016863375.1:n.326-60_326-37del
XR_001741172.2:n.659-60_659-37del
NM_000128.4:c.326-60_326-37del MANE Select NP_000119.1:n.326-60_326-37del
NM_001354804.2:c.326-60_326-37del NP_001341733.1:n.326-60_326-37del