Canonical Allele Identifier: CA2695237820
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896111_154896122del , CM000685.2:g.154896111_154896122del GRCh38
NC_000023.10:g.154124386_154124397del , CM000685.1:g.154124386_154124397del GRCh37
NC_000023.9:g.153777580_153777591del NCBI36
NG_011403.1:g.131604_131615del
NG_011403.2:g.131604_131615del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6386_6397del MANE Select ENSP00000353393.4:p.Lys2129_Gln2132del
ENST00000360256.8:c.6386_6397del ENSP00000353393.4:p.Lys2129_Gln2132del
NM_000132.3:c.6386_6397del NP_000123.1:p.Lys2129_Gln2132del
XM_011531126.1:c.6281_6292del XP_011529428.1:p.Lys2094_Gln2097del
NM_000132.4:c.6386_6397del MANE Select NP_000123.1:p.Lys2129_Gln2132del
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