Canonical Allele Identifier: CA2695237835
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896209_154896211del , CM000685.2:g.154896209_154896211del GRCh38
NC_000023.10:g.154124484_154124486del , CM000685.1:g.154124484_154124486del GRCh37
NC_000023.9:g.153777678_153777680del NCBI36
NG_011403.1:g.131516_131518del
NG_011403.2:g.131516_131518del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6298_6300del MANE Select ENSP00000353393.4:p.Ile2100del
ENST00000360256.8:c.6298_6300del ENSP00000353393.4:p.Ile2100del
NM_000132.3:c.6298_6300del NP_000123.1:p.Ile2100del
XM_011531126.1:c.6193_6195del XP_011529428.1:p.Ile2065del
NM_000132.4:c.6298_6300del MANE Select NP_000123.1:p.Ile2100del
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