Canonical Allele Identifier: CA10529749

Gene: F9

Linked Data

• dbSNP Id: rs768957199
• ExAC: X:138619327 A / AT
• gnomAD v2: X-138619327-A-AT
• MyVariant Identifiers: chrX:g.138619327_138619328insT (hg19) ; chrX:g.139537168_139537169insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537168_139537169insT , CM000685.2:g.139537168_139537169insT	GRCh38
NC_000023.10:g.138619327_138619328insT , CM000685.1:g.138619327_138619328insT	GRCh37
NC_000023.9:g.138446993_138446994insT	NCBI36
NG_007994.1:g.11433_11434insT , LRG_556:g.11433_11434insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.247_248insT MANE Select	ENSP00000218099.2:p.Arg83MetfsTer4
ENST00000218099.6:c.247_248insT	ENSP00000218099.2:p.Arg83MetfsTer4
ENST00000394090.2:c.247_248insT	ENSP00000377650.2:p.Arg83MetfsTer4
ENST00000479617.2:n.241+13_241+14insT
NM_000133.3:c.247_248insT , LRG_556t1:c.247_248insT	NP_000124.1:p.Arg83MetfsTer4
NM_001313913.1:c.247_248insT	NP_001300842.1:p.Arg83MetfsTer4
XM_005262397.3:c.247_248insT	XP_005262454.1:p.Arg83MetfsTer4
XM_005262397.4:c.247_248insT	XP_005262454.1:p.Arg83MetfsTer4
NM_000133.4:c.247_248insT MANE Select	NP_000124.1:p.Arg83MetfsTer4
NM_001313913.2:c.247_248insT	NP_001300842.1:p.Arg83MetfsTer4