Canonical Allele Identifier: CA2695237203
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154947751_154947754del , CM000685.2:g.154947751_154947754del GRCh38
NC_000023.10:g.154176026_154176029del , CM000685.1:g.154176026_154176029del GRCh37
NC_000023.9:g.153829220_153829223del NCBI36
NG_011403.1:g.79973_79976del
NG_011403.2:g.79973_79976del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.2060_2063del MANE Select ENSP00000353393.4:p.Leu687ProfsTer?
ENST00000647125.1:c.*1779+6141_*1779+6144del ENSP00000496062.1:n.*1779+6141_*1779+6144...
ENST00000360256.8:c.2060_2063del ENSP00000353393.4:p.Leu687ProfsTer?
NM_000132.3:c.2060_2063del NP_000123.1:p.Leu687ProfsTer?
XM_011531126.1:c.1955_1958del XP_011529428.1:p.Leu652ProfsTer?
NM_000132.4:c.2060_2063del MANE Select NP_000123.1:p.Leu687ProfsTer?