Canonical Allele Identifier: CA872122347

Gene: F9

Linked Data

• dbSNP Id: rs1202634089
• gnomAD v3: X-139551115-GCTGAGACTGTTTTTC-G
• gnomAD v4: X-139551115-GCTGAGACTGTTTTTC-G
• MyVariant Identifiers: chrX:g.138633275_138633289del (hg19) ; chrX:g.139551116_139551130del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551120_139551134del , CM000685.2:g.139551120_139551134del	GRCh38
NC_000023.10:g.138633279_138633293del , CM000685.1:g.138633279_138633293del	GRCh37
NC_000023.9:g.138460945_138460959del	NCBI36
NG_007994.1:g.25385_25399del , LRG_556:g.25385_25399del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.579_593del MANE Select	ENSP00000218099.2:p.Glu193_Pro197del
ENST00000643157.1:n.1246_1260del
ENST00000218099.6:c.579_593del	ENSP00000218099.2:p.Glu193_Pro197del
ENST00000394090.2:c.465_479del	ENSP00000377650.2:p.Glu155_Pro159del
NM_000133.3:c.579_593del , LRG_556t1:c.579_593del	NP_000124.1:p.Glu193_Pro197del
NM_001313913.1:c.465_479del	NP_001300842.1:p.Glu155_Pro159del
XM_005262397.3:c.450_464del	XP_005262454.1:p.Glu150_Pro154del
XM_005262397.4:c.450_464del	XP_005262454.1:p.Glu150_Pro154del
NM_000133.4:c.579_593del MANE Select	NP_000124.1:p.Glu193_Pro197del
NM_001313913.2:c.465_479del	NP_001300842.1:p.Glu155_Pro159del