Canonical Allele Identifier: CA2695236230

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560761_139560764del , CM000685.2:g.139560761_139560764del	GRCh38
NC_000023.10:g.138642920_138642923del , CM000685.1:g.138642920_138642923del	GRCh37
NC_000023.9:g.138470586_138470589del	NCBI36
NG_007994.1:g.35026_35029del , LRG_556:g.35026_35029del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.744_747del MANE Select	ENSP00000218099.2:p.Asp249HisfsTer14
ENST00000643157.1:n.1411_1414del
ENST00000218099.6:c.744_747del	ENSP00000218099.2:p.Asp249HisfsTer14
ENST00000394090.2:c.630_633del	ENSP00000377650.2:p.Asp211HisfsTer14
NM_000133.3:c.744_747del , LRG_556t1:c.744_747del	NP_000124.1:p.Asp249HisfsTer14
NM_001313913.1:c.630_633del	NP_001300842.1:p.Asp211HisfsTer14
XM_005262397.3:c.615_618del	XP_005262454.1:p.Asp206HisfsTer14
XM_005262397.4:c.615_618del	XP_005262454.1:p.Asp206HisfsTer14
NM_000133.4:c.744_747del MANE Select	NP_000124.1:p.Asp249HisfsTer14
NM_001313913.2:c.630_633del	NP_001300842.1:p.Asp211HisfsTer14