Canonical Allele Identifier: CA2695237985
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904082_154904083del , CM000685.2:g.154904082_154904083del GRCh38
NC_000023.10:g.154132357_154132358del , CM000685.1:g.154132357_154132358del GRCh37
NC_000023.9:g.153785551_153785552del NCBI36
NG_011403.1:g.123641_123642del
NG_011403.2:g.123641_123642del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5821_5822del MANE Select ENSP00000353393.4:p.Asn1941TrpfsTer29
ENST00000360256.8:c.5821_5822del ENSP00000353393.4:p.Asn1941TrpfsTer29
NM_000132.3:c.5821_5822del NP_000123.1:p.Asn1941TrpfsTer29
XM_011531126.1:c.5716_5717del XP_011529428.1:p.Asn1906TrpfsTer29
NM_000132.4:c.5821_5822del MANE Select NP_000123.1:p.Asn1941TrpfsTer29