Canonical Allele Identifier: CA1139667898
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904050dup , CM000685.2:g.154904050dup GRCh38
NC_000023.10:g.154132325dup , CM000685.1:g.154132325dup GRCh37
NC_000023.9:g.153785519dup NCBI36
NG_011403.1:g.123674dup
NG_011403.2:g.123674dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5854dup MANE Select ENSP00000353393.4:p.Val1952GlyfsTer19
ENST00000360256.8:c.5854dup ENSP00000353393.4:p.Val1952GlyfsTer19
NM_000132.3:c.5854dup NP_000123.1:p.Val1952GlyfsTer19
XM_011531126.1:c.5749dup XP_011529428.1:p.Val1917GlyfsTer19
NM_000132.4:c.5854dup MANE Select NP_000123.1:p.Val1952GlyfsTer19
Search 100 bp 5'
Search 100 bp 3'