Canonical Allele Identifier: CA2764868883
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186271707_186271708dup , CM000666.2:g.186271707_186271708dup GRCh38
NC_000004.11:g.187192861_187192862dup , CM000666.1:g.187192861_187192862dup GRCh37
NC_000004.10:g.187429855_187429856dup NCBI36
NG_008051.1:g.10744_10745dup , LRG_583:g.10744_10745dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.154_155dup MANE Select ENSP00000384957.2:p.His53ThrfsTer27
ENST00000264692.8:c.154_155dup ENSP00000264692.5:p.His53ThrfsTer27
ENST00000403665.6:c.154_155dup ENSP00000384957.2:p.His53ThrfsTer27
ENST00000492972.6:c.154_155dup ENSP00000424479.1:p.His53ThrfsTer27
NM_000128.3:c.154_155dup , LRG_583t1:c.154_155dup NP_000119.1:p.His53ThrfsTer27
XM_005262821.2:c.154_155dup XP_005262878.1:p.His53ThrfsTer27
XM_005262822.2:c.154_155dup XP_005262879.1:p.His53ThrfsTer27
XM_005262823.2:c.154_155dup XP_005262880.1:p.His53ThrfsTer27
XM_005262824.1:c.154_155dup XP_005262881.1:p.His53ThrfsTer27
XM_006714137.1:c.154_155dup XP_006714200.1:p.His53ThrfsTer27
XR_938706.1:n.506_507dup
XR_938707.1:n.506_507dup
NM_001354804.1:c.154_155dup NP_001341733.1:p.His53ThrfsTer27
XM_005262821.4:c.154_155dup XP_005262878.1:p.His53ThrfsTer27
XM_005262822.4:c.154_155dup XP_005262879.1:p.His53ThrfsTer27
XM_005262823.4:c.154_155dup XP_005262880.1:p.His53ThrfsTer27
XM_006714137.3:c.154_155dup XP_006714200.1:p.His53ThrfsTer27
XM_017007884.2:c.154_155dup XP_016863373.1:p.His53ThrfsTer27
XM_017007885.2:c.154_155dup XP_016863374.1:p.His53ThrfsTer27
XM_017007886.2:c.154_155dup XP_016863375.1:p.His53ThrfsTer27
XR_001741172.2:n.487_488dup
NM_000128.4:c.154_155dup MANE Select NP_000119.1:p.His53ThrfsTer27
NM_001354804.2:c.154_155dup NP_001341733.1:p.His53ThrfsTer27