Canonical Allele Identifier: CA2695236284

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561592del , CM000685.2:g.139561592del	GRCh38
NC_000023.10:g.138643751del , CM000685.1:g.138643751del	GRCh37
NC_000023.9:g.138471417del	NCBI36
NG_007994.1:g.35857del , LRG_556:g.35857del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.907del MANE Select	ENSP00000218099.2:p.His303ThrfsTer23
ENST00000643157.1:n.1574del
ENST00000218099.6:c.907del	ENSP00000218099.2:p.His303ThrfsTer23
ENST00000394090.2:c.793del	ENSP00000377650.2:p.His265ThrfsTer23
NM_000133.3:c.907del , LRG_556t1:c.907del	NP_000124.1:p.His303ThrfsTer23
NM_001313913.1:c.793del	NP_001300842.1:p.His265ThrfsTer23
XM_005262397.3:c.778del	XP_005262454.1:p.His260ThrfsTer23
XM_005262397.4:c.778del	XP_005262454.1:p.His260ThrfsTer23
NM_000133.4:c.907del MANE Select	NP_000124.1:p.His303ThrfsTer23
NM_001313913.2:c.793del	NP_001300842.1:p.His265ThrfsTer23