Canonical Allele Identifier: CA2695237235
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953953del , CM000685.2:g.154953953del GRCh38
NC_000023.10:g.154182228del , CM000685.1:g.154182228del GRCh37
NC_000023.9:g.153835422del NCBI36
NG_011403.1:g.73774del
NG_011403.2:g.73774del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1845del MANE Select ENSP00000353393.4:p.Asn616IlefsTer?
ENST00000647125.1:c.*1721del ENSP00000496062.1:n.*1721del
ENST00000360256.8:c.1845del ENSP00000353393.4:p.Asn616IlefsTer?
NM_000132.3:c.1845del NP_000123.1:p.Asn616IlefsTer?
XM_011531126.1:c.1740del XP_011529428.1:p.Asn581IlefsTer?
NM_000132.4:c.1845del MANE Select NP_000123.1:p.Asn616IlefsTer?