Canonical Allele Identifier: CA2694839893

Gene: F9

Linked Data

• gnomAD v4: X-139562027-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562030del , CM000685.2:g.139562030del	GRCh38
NC_000023.10:g.138644189del , CM000685.1:g.138644189del	GRCh37
NC_000023.9:g.138471855del	NCBI36
NG_007994.1:g.36295del , LRG_556:g.36295del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1345del MANE Select	ENSP00000218099.2:p.Arg449GlyfsTer?
ENST00000643157.1:n.1723+289del
ENST00000218099.6:c.1345del	ENSP00000218099.2:p.Arg449GlyfsTer?
ENST00000394090.2:c.1231del	ENSP00000377650.2:p.Arg411GlyfsTer?
NM_000133.3:c.1345del , LRG_556t1:c.1345del	NP_000124.1:p.Arg449GlyfsTer?
NM_001313913.1:c.1231del	NP_001300842.1:p.Arg411GlyfsTer?
XM_005262397.3:c.1216del	XP_005262454.1:p.Arg406GlyfsTer?
XM_005262397.4:c.1216del	XP_005262454.1:p.Arg406GlyfsTer?
NM_000133.4:c.1345del MANE Select	NP_000124.1:p.Arg449GlyfsTer?
NM_001313913.2:c.1231del	NP_001300842.1:p.Arg411GlyfsTer?