Canonical Allele Identifier: CA2982921033
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280339dup , CM000666.2:g.186280339dup GRCh38
NC_000004.11:g.187201493dup , CM000666.1:g.187201493dup GRCh37
NC_000004.10:g.187438487dup NCBI36
NG_008051.1:g.19376dup , LRG_583:g.19376dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.982dup MANE Select ENSP00000384957.2:p.Gln328ProfsTer?
ENST00000264692.8:c.820dup ENSP00000264692.5:p.Gln274ProfsTer?
ENST00000403665.6:c.982dup ENSP00000384957.2:p.Gln328ProfsTer?
ENST00000452239.1:c.429dup
NM_000128.3:c.982dup , LRG_583t1:c.982dup NP_000119.1:p.Gln328ProfsTer?
XM_005262821.2:c.982dup XP_005262878.1:p.Gln328ProfsTer?
XM_005262822.2:c.982dup XP_005262879.1:p.Gln328ProfsTer?
XM_005262823.2:c.712dup XP_005262880.1:p.Gln238ProfsTer?
XM_005262824.1:c.982dup XP_005262881.1:p.Gln328ProfsTer?
XM_006714137.1:c.934dup XP_006714200.1:p.Gln312ProfsTer?
XR_938706.1:n.1334dup
XR_938707.1:n.1334dup
XM_005262821.4:c.982dup XP_005262878.1:p.Gln328ProfsTer?
XM_005262822.4:c.982dup XP_005262879.1:p.Gln328ProfsTer?
XM_005262823.4:c.712dup XP_005262880.1:p.Gln238ProfsTer?
XM_006714137.3:c.934dup XP_006714200.1:p.Gln312ProfsTer?
XM_017007884.2:c.982dup XP_016863373.1:p.Gln328ProfsTer?
XM_017007885.2:c.982dup XP_016863374.1:p.Gln328ProfsTer?
XM_017007886.2:c.982dup XP_016863375.1:p.Gln328ProfsTer?
XR_001741172.2:n.1315dup
NM_000128.4:c.982dup MANE Select NP_000119.1:p.Gln328ProfsTer?