Canonical Allele Identifier: CA2672902721
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285579del , CM000666.2:g.186285579del GRCh38
NC_000004.11:g.187206733del , CM000666.1:g.187206733del GRCh37
NC_000004.10:g.187443727del NCBI36
NG_008051.1:g.24616del , LRG_583:g.24616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1305-59del MANE Select ENSP00000384957.2:n.1305-59del
ENST00000264692.8:c.1143-59del ENSP00000264692.5:n.1143-59del
ENST00000403665.6:c.1305-59del ENSP00000384957.2:n.1305-59del
NM_000128.3:c.1305-59del , LRG_583t1:c.1305-59del NP_000119.1:n.1305-59del
XM_005262821.2:c.1308-59del XP_005262878.1:n.1308-59del
XM_005262822.2:c.1308-59del XP_005262879.1:n.1308-59del
XM_005262823.2:c.1038-59del XP_005262880.1:n.1038-59del
XM_005262824.1:c.1308-59del XP_005262881.1:n.1308-59del
XM_006714137.1:c.1260-59del XP_006714200.1:n.1260-59del
XR_938706.1:n.1713-59del
XR_938707.1:n.1713-59del
XM_005262821.4:c.1308-59del XP_005262878.1:n.1308-59del
XM_005262822.4:c.1308-59del XP_005262879.1:n.1308-59del
XM_005262823.4:c.1038-59del XP_005262880.1:n.1038-59del
XM_006714137.3:c.1260-59del XP_006714200.1:n.1260-59del
XR_001741172.2:n.1779-59del
NM_000128.4:c.1305-59del MANE Select NP_000119.1:n.1305-59del