Canonical Allele Identifier: CA2695237890
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902137del , CM000685.2:g.154902137del GRCh38
NC_000023.10:g.154130412del , CM000685.1:g.154130412del GRCh37
NC_000023.9:g.153783606del NCBI36
NG_011403.1:g.125588del
NG_011403.2:g.125588del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6030del MANE Select ENSP00000353393.4:p.Ala2012LeufsTer18
ENST00000360256.8:c.6030del ENSP00000353393.4:p.Ala2012LeufsTer18
NM_000132.3:c.6030del NP_000123.1:p.Ala2012LeufsTer18
XM_011531126.1:c.5925del XP_011529428.1:p.Ala1977LeufsTer18
NM_000132.4:c.6030del MANE Select NP_000123.1:p.Ala2012LeufsTer18
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