Canonical Allele Identifier: CA2695237959
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928879dup , CM000685.2:g.154928879dup GRCh38
NC_000023.10:g.154157154dup , CM000685.1:g.154157154dup GRCh37
NC_000023.9:g.153810348dup NCBI36
NG_011403.1:g.98845dup
NG_011403.2:g.98845dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4911dup MANE Select ENSP00000353393.4:p.Lys1638Ter
ENST00000360256.8:c.4911dup ENSP00000353393.4:p.Lys1638Ter
NM_000132.3:c.4911dup NP_000123.1:p.Lys1638Ter
XM_011531126.1:c.4806dup XP_011529428.1:p.Lys1603Ter
NM_000132.4:c.4911dup MANE Select NP_000123.1:p.Lys1638Ter
Search 100 bp 5'
Search 100 bp 3'