Canonical Allele Identifier: CA873344580
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1435522526
MyVariant Identifiers: chrX:g.154966563del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966564del , CM000685.2:g.154966564del GRCh38
NC_000023.10:g.154194839del , CM000685.1:g.154194839del GRCh37
NC_000023.9:g.153848033del NCBI36
NG_011403.1:g.61161del
NG_011403.2:g.61161del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1134del MANE Select ENSP00000353393.4:p.Arg378SerfsTer?
ENST00000647125.1:c.*1010del ENSP00000496062.1:n.*1010del
ENST00000360256.8:c.1134del ENSP00000353393.4:p.Arg378SerfsTer?
NM_000132.3:c.1134del NP_000123.1:p.Arg378SerfsTer?
XM_011531126.1:c.1029del XP_011529428.1:p.Arg343SerfsTer?
NM_000132.4:c.1134del MANE Select NP_000123.1:p.Arg378SerfsTer?