Canonical Allele Identifier: CA2695237972
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904040_154904045del , CM000685.2:g.154904040_154904045del GRCh38
NC_000023.10:g.154132315_154132320del , CM000685.1:g.154132315_154132320del GRCh37
NC_000023.9:g.153785509_153785514del NCBI36
NG_011403.1:g.123681_123686del
NG_011403.2:g.123681_123686del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5861_5866del MANE Select ENSP00000353393.4:p.Ala1954_Gln1955del
ENST00000360256.8:c.5861_5866del ENSP00000353393.4:p.Ala1954_Gln1955del
NM_000132.3:c.5861_5866del NP_000123.1:p.Ala1954_Gln1955del
XM_011531126.1:c.5756_5761del XP_011529428.1:p.Ala1919_Gln1920del
NM_000132.4:c.5861_5866del MANE Select NP_000123.1:p.Ala1954_Gln1955del