Canonical Allele Identifier: CA2672902445
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280074_186280076del , CM000666.2:g.186280074_186280076del GRCh38
NC_000004.11:g.187201228_187201230del , CM000666.1:g.187201228_187201230del GRCh37
NC_000004.10:g.187438222_187438224del NCBI36
NG_008051.1:g.19111_19113del , LRG_583:g.19111_19113del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.818_820del MANE Select ENSP00000384957.2:p.Lys273_Ala274delinsThr
ENST00000264692.8:c.656_658del ENSP00000264692.5:p.Lys219_Ala220delinsThr
ENST00000403665.6:c.818_820del ENSP00000384957.2:p.Lys273_Ala274delinsThr
ENST00000452239.1:c.265_267del
NM_000128.3:c.818_820del , LRG_583t1:c.818_820del NP_000119.1:p.Lys273_Ala274delinsThr
XM_005262821.2:c.818_820del XP_005262878.1:p.Lys273_Ala274delinsThr
XM_005262822.2:c.818_820del XP_005262879.1:p.Lys273_Ala274delinsThr
XM_005262823.2:c.548_550del XP_005262880.1:p.Lys183_Ala184delinsThr
XM_005262824.1:c.818_820del XP_005262881.1:p.Lys273_Ala274delinsThr
XM_006714137.1:c.818_820del XP_006714200.1:p.Lys273_Ala274delinsThr
XR_938706.1:n.1170_1172del
XR_938707.1:n.1170_1172del
XM_005262821.4:c.818_820del XP_005262878.1:p.Lys273_Ala274delinsThr
XM_005262822.4:c.818_820del XP_005262879.1:p.Lys273_Ala274delinsThr
XM_005262823.4:c.548_550del XP_005262880.1:p.Lys183_Ala184delinsThr
XM_006714137.3:c.818_820del XP_006714200.1:p.Lys273_Ala274delinsThr
XM_017007884.2:c.818_820del XP_016863373.1:p.Lys273_Ala274delinsThr
XM_017007885.2:c.818_820del XP_016863374.1:p.Lys273_Ala274delinsThr
XM_017007886.2:c.818_820del XP_016863375.1:p.Lys273_Ala274delinsThr
XR_001741172.2:n.1151_1153del
NM_000128.4:c.818_820del MANE Select NP_000119.1:p.Lys273_Ala274delinsThr