Canonical Allele Identifier: CA2695236360

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561836_139561839del , CM000685.2:g.139561836_139561839del	GRCh38
NC_000023.10:g.138643995_138643998del , CM000685.1:g.138643995_138643998del	GRCh37
NC_000023.9:g.138471661_138471664del	NCBI36
NG_007994.1:g.36101_36104del , LRG_556:g.36101_36104del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1151_1154del MANE Select	ENSP00000218099.2:p.Arg384LeufsTer?
ENST00000643157.1:n.1723+95_1723+98del
ENST00000218099.6:c.1151_1154del	ENSP00000218099.2:p.Arg384LeufsTer?
ENST00000394090.2:c.1037_1040del	ENSP00000377650.2:p.Arg346LeufsTer?
NM_000133.3:c.1151_1154del , LRG_556t1:c.1151_1154del	NP_000124.1:p.Arg384LeufsTer?
NM_001313913.1:c.1037_1040del	NP_001300842.1:p.Arg346LeufsTer?
XM_005262397.3:c.1022_1025del	XP_005262454.1:p.Arg341LeufsTer?
XM_005262397.4:c.1022_1025del	XP_005262454.1:p.Arg341LeufsTer?
NM_000133.4:c.1151_1154del MANE Select	NP_000124.1:p.Arg384LeufsTer?
NM_001313913.2:c.1037_1040del	NP_001300842.1:p.Arg346LeufsTer?