Canonical Allele Identifier: CA2695237951
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903976del , CM000685.2:g.154903976del GRCh38
NC_000023.10:g.154132251del , CM000685.1:g.154132251del GRCh37
NC_000023.9:g.153785445del NCBI36
NG_011403.1:g.123750del
NG_011403.2:g.123750del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5930del MANE Select ENSP00000353393.4:p.Phe1977SerfsTer?
ENST00000360256.8:c.5930del ENSP00000353393.4:p.Phe1977SerfsTer?
NM_000132.3:c.5930del NP_000123.1:p.Phe1977SerfsTer?
XM_011531126.1:c.5825del XP_011529428.1:p.Phe1942SerfsTer?
NM_000132.4:c.5930del MANE Select NP_000123.1:p.Phe1977SerfsTer?