Canonical Allele Identifier: CA872115997

Gene: F9

Linked Data

• dbSNP Id: rs1384741616
• MyVariant Identifiers: chrX:g.138619241_138619245del (hg19) ; chrX:g.139537082_139537086del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537082_139537086del , CM000685.2:g.139537082_139537086del	GRCh38
NC_000023.10:g.138619241_138619245del , CM000685.1:g.138619241_138619245del	GRCh37
NC_000023.9:g.138446907_138446911del	NCBI36
NG_007994.1:g.11347_11351del , LRG_556:g.11347_11351del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.161_165del MANE Select	ENSP00000218099.2:p.Glu54GlyfsTer6
ENST00000218099.6:c.161_165del	ENSP00000218099.2:p.Glu54GlyfsTer6
ENST00000394090.2:c.161_165del	ENSP00000377650.2:p.Glu54GlyfsTer6
ENST00000479617.2:n.168_172del
NM_000133.3:c.161_165del , LRG_556t1:c.161_165del	NP_000124.1:p.Glu54GlyfsTer6
NM_001313913.1:c.161_165del	NP_001300842.1:p.Glu54GlyfsTer6
XM_005262397.3:c.161_165del	XP_005262454.1:p.Glu54GlyfsTer6
XM_005262397.4:c.161_165del	XP_005262454.1:p.Glu54GlyfsTer6
NM_000133.4:c.161_165del MANE Select	NP_000124.1:p.Glu54GlyfsTer6
NM_001313913.2:c.161_165del	NP_001300842.1:p.Glu54GlyfsTer6