Canonical Allele Identifier: CA2672902499
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280512_186280526del , CM000666.2:g.186280512_186280526del GRCh38
NC_000004.11:g.187201666_187201680del , CM000666.1:g.187201666_187201680del GRCh37
NC_000004.10:g.187438660_187438674del NCBI36
NG_008051.1:g.19549_19563del , LRG_583:g.19549_19563del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1067_1081del MANE Select ENSP00000384957.2:p.Pro356_Leu360del
ENST00000264692.8:c.905_919del ENSP00000264692.5:p.Pro302_Leu306del
ENST00000403665.6:c.1067_1081del ENSP00000384957.2:p.Pro356_Leu360del
ENST00000452239.1:c.514_528del
NM_000128.3:c.1067_1081del , LRG_583t1:c.1067_1081del NP_000119.1:p.Pro356_Leu360del
XM_005262821.2:c.1070_1084del XP_005262878.1:p.Pro357_Leu361del
XM_005262822.2:c.1070_1084del XP_005262879.1:p.Pro357_Leu361del
XM_005262823.2:c.800_814del XP_005262880.1:p.Pro267_Leu271del
XM_005262824.1:c.1070_1084del XP_005262881.1:p.Pro357_Leu361del
XM_006714137.1:c.1022_1036del XP_006714200.1:p.Pro341_Leu345del
XR_938706.1:n.1422_1436del
XR_938707.1:n.1422_1436del
XM_005262821.4:c.1070_1084del XP_005262878.1:p.Pro357_Leu361del
XM_005262822.4:c.1070_1084del XP_005262879.1:p.Pro357_Leu361del
XM_005262823.4:c.800_814del XP_005262880.1:p.Pro267_Leu271del
XM_006714137.3:c.1022_1036del XP_006714200.1:p.Pro341_Leu345del
XM_017007884.2:c.1070_1084del XP_016863373.1:p.Pro357_Leu361del
XM_017007885.2:c.1070_1084del XP_016863374.1:p.Pro357_Leu361del
XM_017007886.2:c.1067_1081del XP_016863375.1:p.Pro356_Leu360del
XR_001741172.2:n.1488_1502del
NM_000128.4:c.1067_1081del MANE Select NP_000119.1:p.Pro356_Leu360del