Canonical Allele Identifier: CA2695237887
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928627dup , CM000685.2:g.154928627dup GRCh38
NC_000023.10:g.154156902dup , CM000685.1:g.154156902dup GRCh37
NC_000023.9:g.153810096dup NCBI36
NG_011403.1:g.99097dup
NG_011403.2:g.99097dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5163dup MANE Select ENSP00000353393.4:p.Val1722SerfsTer11
ENST00000360256.8:c.5163dup ENSP00000353393.4:p.Val1722SerfsTer11
NM_000132.3:c.5163dup NP_000123.1:p.Val1722SerfsTer11
XM_011531126.1:c.5058dup XP_011529428.1:p.Val1687SerfsTer11
NM_000132.4:c.5163dup MANE Select NP_000123.1:p.Val1722SerfsTer11
Search 100 bp 5'
Search 100 bp 3'