Canonical Allele Identifier: CA2695168809
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154928898-GCTGCTA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928899_154928904del , CM000685.2:g.154928899_154928904del GRCh38
NC_000023.10:g.154157174_154157179del , CM000685.1:g.154157174_154157179del GRCh37
NC_000023.9:g.153810368_153810373del NCBI36
NG_011403.1:g.98820_98825del
NG_011403.2:g.98820_98825del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4886_4891del MANE Select ENSP00000353393.4:p.Ile1629_Ala1631delinsThr
ENST00000360256.8:c.4886_4891del ENSP00000353393.4:p.Ile1629_Ala1631delinsThr
NM_000132.3:c.4886_4891del NP_000123.1:p.Ile1629_Ala1631delinsThr
XM_011531126.1:c.4781_4786del XP_011529428.1:p.Ile1594_Ala1596delinsThr
NM_000132.4:c.4886_4891del MANE Select NP_000123.1:p.Ile1629_Ala1631delinsThr
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