Canonical Allele Identifier: CA255462

Gene: F9

Linked Data

• ClinVar Variation Id: 10667
• ClinVar RCV Id: RCV000011412
• dbSNP Id: rs587776736
• MyVariant Identifiers: chrX:g.138633240_138633241del (hg19) ; chrX:g.139551081_139551082del (hg38)
• PubMed: PMID:15266608

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551081_139551082del , CM000685.2:g.139551081_139551082del	GRCh38
NC_000023.10:g.138633240_138633241del , CM000685.1:g.138633240_138633241del	GRCh37
NC_000023.9:g.138460906_138460907del	NCBI36
NG_007994.1:g.25346_25347del , LRG_556:g.25346_25347del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.540_541del MANE Select	ENSP00000218099.2:p.Arg180SerfsTer8
ENST00000643157.1:n.1207_1208del
ENST00000218099.6:c.540_541del	ENSP00000218099.2:p.Arg180SerfsTer8
ENST00000394090.2:c.426_427del	ENSP00000377650.2:p.Arg142SerfsTer8
NM_000133.3:c.540_541del , LRG_556t1:c.540_541del	NP_000124.1:p.Arg180SerfsTer8
NM_001313913.1:c.426_427del	NP_001300842.1:p.Arg142SerfsTer8
XM_005262397.3:c.411_412del	XP_005262454.1:p.Arg137SerfsTer8
XM_005262397.4:c.411_412del	XP_005262454.1:p.Arg137SerfsTer8
NM_000133.4:c.540_541del MANE Select	NP_000124.1:p.Arg180SerfsTer8
NM_001313913.2:c.426_427del	NP_001300842.1:p.Arg142SerfsTer8