Canonical Allele Identifier: CA2695238489
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997069_154997074del , CM000685.2:g.154997069_154997074del GRCh38
NC_000023.10:g.154225344_154225349del , CM000685.1:g.154225344_154225349del GRCh37
NC_000023.9:g.153878538_153878543del NCBI36
NG_011403.1:g.30653_30658del
NG_011403.2:g.30653_30658del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.290_295del MANE Select ENSP00000353393.4:p.Ala97_Glu98del
ENST00000647125.1:c.*76_*81del ENSP00000496062.1:n.*76_*81del
ENST00000360256.8:c.290_295del ENSP00000353393.4:p.Ala97_Glu98del
ENST00000423959.5:c.185_190del ENSP00000409446.1:p.Ala62_Glu63del
ENST00000453950.1:c.272_277del ENSP00000389153.1:p.Ala91_Glu92del
NM_000132.3:c.290_295del NP_000123.1:p.Ala97_Glu98del
XM_011531126.1:c.185_190del XP_011529428.1:p.Ala62_Glu63del
NM_000132.4:c.290_295del MANE Select NP_000123.1:p.Ala97_Glu98del