Canonical Allele Identifier: CA2695237834
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896194dup , CM000685.2:g.154896194dup GRCh38
NC_000023.10:g.154124469dup , CM000685.1:g.154124469dup GRCh37
NC_000023.9:g.153777663dup NCBI36
NG_011403.1:g.131530dup
NG_011403.2:g.131530dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6312dup MANE Select ENSP00000353393.4:p.Thr2105AspfsTer21
ENST00000360256.8:c.6312dup ENSP00000353393.4:p.Thr2105AspfsTer21
NM_000132.3:c.6312dup NP_000123.1:p.Thr2105AspfsTer21
XM_011531126.1:c.6207dup XP_011529428.1:p.Thr2070AspfsTer21
NM_000132.4:c.6312dup MANE Select NP_000123.1:p.Thr2105AspfsTer21
Search 100 bp 5'
Search 100 bp 3'