Canonical Allele Identifier: CA1519934228
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276376C= , CM000666.2:g.186276376C= GRCh38
NC_000004.11:g.187197530C= , CM000666.1:g.187197530C= GRCh37
NC_000004.10:g.187434524C= NCBI36
NG_008051.1:g.15413C= , LRG_583:g.15413C=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.741C= MANE Select ENSP00000384957.2:p.Pro247=
ENST00000264692.8:c.579C= ENSP00000264692.5:p.Pro193=
ENST00000403665.6:c.741C= ENSP00000384957.2:p.Pro247=
ENST00000452239.1:c.188C=
NM_000128.3:c.741C= , LRG_583t1:c.741C= NP_000119.1:p.Pro247=
XM_005262821.2:c.741C= XP_005262878.1:p.Pro247=
XM_005262822.2:c.741C= XP_005262879.1:p.Pro247=
XM_005262823.2:c.485+2101C= XP_005262880.1:n.485+2101C=
XM_005262824.1:c.741C= XP_005262881.1:p.Pro247=
XM_006714137.1:c.741C= XP_006714200.1:p.Pro247=
XR_938706.1:n.1093C=
XR_938707.1:n.1093C=
XM_005262821.4:c.741C= XP_005262878.1:p.Pro247=
XM_005262822.4:c.741C= XP_005262879.1:p.Pro247=
XM_005262823.4:c.485+2101C= XP_005262880.1:n.485+2101C=
XM_006714137.3:c.741C= XP_006714200.1:p.Pro247=
XM_017007884.2:c.741C= XP_016863373.1:p.Pro247=
XM_017007885.2:c.741C= XP_016863374.1:p.Pro247=
XM_017007886.2:c.741C= XP_016863375.1:p.Pro247=
XR_001741172.2:n.1074C=
NM_000128.4:c.741C= MANE Select NP_000119.1:p.Pro247=