Canonical Allele Identifier: CA1519938802

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186286423C= , CM000666.2:g.186286423C= GRCh38
NC_000004.11:g.187207577C= , CM000666.1:g.187207577C= GRCh37
NC_000004.10:g.187444571C= NCBI36
NG_008051.1:g.25460C= , LRG_583:g.25460C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1489C= (F11) MANE Select ENSP00000384957.2:p.Arg497=
ENST00000264691.4:c.176+610C= (F11)
ENST00000264692.8:c.1327C= (F11) ENSP00000264692.5:p.Arg443=
ENST00000403665.6:c.1489C= (F11) ENSP00000384957.2:p.Arg497=
NM_000128.3:c.1489C= , LRG_583t1:c.1489C= (F11) NP_000119.1:p.Arg497=
NR_033900.1:n.1067-157G= (F11-AS1)
XM_005262821.2:c.1492C= (F11) XP_005262878.1:p.Arg498=
XM_005262822.2:c.1483+610C= (F11) XP_005262879.1:n.1483+610C=
XM_005262823.2:c.1222C= (F11) XP_005262880.1:p.Arg408=
XM_005262824.1:c.1484-123C= (F11) XP_005262881.1:n.1484-123C=
XM_006714137.1:c.1444C= (F11) XP_006714200.1:p.Arg482=
XR_938706.1:n.1897C= (F11)
XR_938707.1:n.1888+610C= (F11)
XM_005262821.4:c.1492C= (F11) XP_005262878.1:p.Arg498=
XM_005262822.4:c.1483+610C= (F11) XP_005262879.1:n.1483+610C=
XM_005262823.4:c.1222C= (F11) XP_005262880.1:p.Arg408=
XM_006714137.3:c.1444C= (F11) XP_006714200.1:p.Arg482=
XR_001741172.2:n.1963C= (F11)
NM_000128.4:c.1489C= (F11) MANE Select NP_000119.1:p.Arg497=