Canonical Allele Identifier: CA1519940276
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186289291C= , CM000666.2:g.186289291C= GRCh38
NC_000004.11:g.187210445C= , CM000666.1:g.187210445C= GRCh37
NC_000004.10:g.187447439C= NCBI36
NG_008051.1:g.28328C= , LRG_583:g.28328C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.*677C= (F11) MANE Select ENSP00000384957.2:n.*677C=
NM_000128.3:c.*677C= , LRG_583t1:c.*677C= (F11) NP_000119.1:n.*677C=
NR_033900.1:n.492-289G= (F11-AS1)
XM_005262821.2:c.*677C= (F11) XP_005262878.1:n.*677C=
XM_005262822.2:c.*677C= (F11) XP_005262879.1:n.*677C=
XM_005262823.2:c.*677C= (F11) XP_005262880.1:n.*677C=
XM_006714137.1:c.*677C= (F11) XP_006714200.1:n.*677C=
XM_005262821.4:c.*677C= (F11) XP_005262878.1:n.*677C=
XM_005262822.4:c.*677C= (F11) XP_005262879.1:n.*677C=
XM_005262823.4:c.*677C= (F11) XP_005262880.1:n.*677C=
XM_006714137.3:c.*677C= (F11) XP_006714200.1:n.*677C=
NM_000128.4:c.*677C= (F11) MANE Select NP_000119.1:n.*677C=
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