Canonical Allele Identifier: CA2695237957
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903990del , CM000685.2:g.154903990del GRCh38
NC_000023.10:g.154132265del , CM000685.1:g.154132265del GRCh37
NC_000023.9:g.153785459del NCBI36
NG_011403.1:g.123734del
NG_011403.2:g.123734del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5914del MANE Select ENSP00000353393.4:p.Ile1972SerfsTer?
ENST00000360256.8:c.5914del ENSP00000353393.4:p.Ile1972SerfsTer?
NM_000132.3:c.5914del NP_000123.1:p.Ile1972SerfsTer?
XM_011531126.1:c.5809del XP_011529428.1:p.Ile1937SerfsTer?
NM_000132.4:c.5914del MANE Select NP_000123.1:p.Ile1972SerfsTer?