Canonical Allele Identifier: CA2695238118
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904877_154904879del , CM000685.2:g.154904877_154904879del GRCh38
NC_000023.10:g.154133152_154133154del , CM000685.1:g.154133152_154133154del GRCh37
NC_000023.9:g.153786346_153786348del NCBI36
NG_011403.1:g.122848_122850del
NG_011403.2:g.122848_122850del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5521_5523del MANE Select ENSP00000353393.4:p.His1841del
ENST00000360256.8:c.5521_5523del ENSP00000353393.4:p.His1841del
NM_000132.3:c.5521_5523del NP_000123.1:p.His1841del
XM_011531126.1:c.5416_5418del XP_011529428.1:p.His1806del
NM_000132.4:c.5521_5523del MANE Select NP_000123.1:p.His1841del
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