Canonical Allele Identifier: CA2695237352
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966477del , CM000685.2:g.154966477del GRCh38
NC_000023.10:g.154194752del , CM000685.1:g.154194752del GRCh37
NC_000023.9:g.153847946del NCBI36
NG_011403.1:g.61247del
NG_011403.2:g.61247del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1220del MANE Select ENSP00000353393.4:p.Ala407ValfsTer11
ENST00000647125.1:c.*1096del ENSP00000496062.1:n.*1096del
ENST00000360256.8:c.1220del ENSP00000353393.4:p.Ala407ValfsTer11
ENST00000483822.2:n.40del
NM_000132.3:c.1220del NP_000123.1:p.Ala407ValfsTer11
XM_011531126.1:c.1115del XP_011529428.1:p.Ala372ValfsTer11
NM_000132.4:c.1220del MANE Select NP_000123.1:p.Ala407ValfsTer11
Search 100 bp 5'
Search 100 bp 3'