Canonical Allele Identifier: CA2695238157
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904986_154904988del , CM000685.2:g.154904986_154904988del GRCh38
NC_000023.10:g.154133261_154133263del , CM000685.1:g.154133261_154133263del GRCh37
NC_000023.9:g.153786455_153786457del NCBI36
NG_011403.1:g.122738_122740del
NG_011403.2:g.122738_122740del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5411_5413del MANE Select ENSP00000353393.4:p.Phe1804del
ENST00000360256.8:c.5411_5413del ENSP00000353393.4:p.Phe1804del
NM_000132.3:c.5411_5413del NP_000123.1:p.Phe1804del
XM_011531126.1:c.5306_5308del XP_011529428.1:p.Phe1769del
NM_000132.4:c.5411_5413del MANE Select NP_000123.1:p.Phe1804del
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