Canonical Allele Identifier: CA3008561330
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903985del , CM000685.2:g.154903985del GRCh38
NC_000023.10:g.154132260del , CM000685.1:g.154132260del GRCh37
NC_000023.9:g.153785454del NCBI36
NG_011403.1:g.123740del
NG_011403.2:g.123740del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5920del MANE Select ENSP00000353393.4:p.Ser1974LeufsTer?
ENST00000360256.8:c.5920del ENSP00000353393.4:p.Ser1974LeufsTer?
NM_000132.3:c.5920del NP_000123.1:p.Ser1974LeufsTer?
XM_011531126.1:c.5815del XP_011529428.1:p.Ser1939LeufsTer?
NM_000132.4:c.5920del MANE Select NP_000123.1:p.Ser1974LeufsTer?