Canonical Allele Identifier: CA2695237906
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928653del , CM000685.2:g.154928653del GRCh38
NC_000023.10:g.154156928del , CM000685.1:g.154156928del GRCh37
NC_000023.9:g.153810122del NCBI36
NG_011403.1:g.99074del
NG_011403.2:g.99074del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5140del MANE Select ENSP00000353393.4:p.Thr1714HisfsTer17
ENST00000360256.8:c.5140del ENSP00000353393.4:p.Thr1714HisfsTer17
NM_000132.3:c.5140del NP_000123.1:p.Thr1714HisfsTer17
XM_011531126.1:c.5035del XP_011529428.1:p.Thr1679HisfsTer17
NM_000132.4:c.5140del MANE Select NP_000123.1:p.Thr1714HisfsTer17
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