Canonical Allele Identifier: CA1519939978
Gene: F11 HGNC NCBI
F11-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186288880T= , CM000666.2:g.186288880T= GRCh38
NC_000004.11:g.187210034T= , CM000666.1:g.187210034T= GRCh37
NC_000004.10:g.187447028T= NCBI36
NG_008051.1:g.27917T= , LRG_583:g.27917T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.*266T= (F11) MANE Select ENSP00000384957.2:n.*266T=
NM_000128.3:c.*266T= , LRG_583t1:c.*266T= (F11) NP_000119.1:n.*266T=
NR_033900.1:n.614A= (F11-AS1)
XM_005262821.2:c.*266T= (F11) XP_005262878.1:n.*266T=
XM_005262822.2:c.*266T= (F11) XP_005262879.1:n.*266T=
XM_005262823.2:c.*266T= (F11) XP_005262880.1:n.*266T=
XM_006714137.1:c.*266T= (F11) XP_006714200.1:n.*266T=
XM_005262821.4:c.*266T= (F11) XP_005262878.1:n.*266T=
XM_005262822.4:c.*266T= (F11) XP_005262879.1:n.*266T=
XM_005262823.4:c.*266T= (F11) XP_005262880.1:n.*266T=
XM_006714137.3:c.*266T= (F11) XP_006714200.1:n.*266T=
NM_000128.4:c.*266T= (F11) MANE Select NP_000119.1:n.*266T=
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