Canonical Allele Identifier: CA2695237257
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957076del , CM000685.2:g.154957076del GRCh38
NC_000023.10:g.154185351del , CM000685.1:g.154185351del GRCh37
NC_000023.9:g.153838545del NCBI36
NG_011403.1:g.70649del
NG_011403.2:g.70649del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1634del MANE Select ENSP00000353393.4:p.Pro545LeufsTer4
ENST00000647125.1:c.*1510del ENSP00000496062.1:n.*1510del
ENST00000360256.8:c.1634del ENSP00000353393.4:p.Pro545LeufsTer4
NM_000132.3:c.1634del NP_000123.1:p.Pro545LeufsTer4
XM_011531126.1:c.1529del XP_011529428.1:p.Pro510LeufsTer4
NM_000132.4:c.1634del MANE Select NP_000123.1:p.Pro545LeufsTer4