Canonical Allele Identifier: CA2695237919
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903919_154903931del , CM000685.2:g.154903919_154903931del GRCh38
NC_000023.10:g.154132194_154132206del , CM000685.1:g.154132194_154132206del GRCh37
NC_000023.9:g.153785388_153785400del NCBI36
NG_011403.1:g.123796_123808del
NG_011403.2:g.123796_123808del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5976_5988del MANE Select ENSP00000353393.4:p.Met1992IlefsTer?
ENST00000360256.8:c.5976_5988del ENSP00000353393.4:p.Met1992IlefsTer?
NM_000132.3:c.5976_5988del NP_000123.1:p.Met1992IlefsTer?
XM_011531126.1:c.5871_5883del XP_011529428.1:p.Met1957IlefsTer?
NM_000132.4:c.5976_5988del MANE Select NP_000123.1:p.Met1992IlefsTer?