Canonical Allele Identifier: CA2695237939
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928751del , CM000685.2:g.154928751del GRCh38
NC_000023.10:g.154157026del , CM000685.1:g.154157026del GRCh37
NC_000023.9:g.153810220del NCBI36
NG_011403.1:g.98975del
NG_011403.2:g.98975del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5041del MANE Select ENSP00000353393.4:p.Ile1681LeufsTer11
ENST00000360256.8:c.5041del ENSP00000353393.4:p.Ile1681LeufsTer11
NM_000132.3:c.5041del NP_000123.1:p.Ile1681LeufsTer11
XM_011531126.1:c.4936del XP_011529428.1:p.Ile1646LeufsTer11
NM_000132.4:c.5041del MANE Select NP_000123.1:p.Ile1681LeufsTer11
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