Canonical Allele Identifier: CA2695236293

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561623del , CM000685.2:g.139561623del	GRCh38
NC_000023.10:g.138643782del , CM000685.1:g.138643782del	GRCh37
NC_000023.9:g.138471448del	NCBI36
NG_007994.1:g.35888del , LRG_556:g.35888del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.938del MANE Select	ENSP00000218099.2:p.Asn313ThrfsTer13
ENST00000643157.1:n.1605del
ENST00000218099.6:c.938del	ENSP00000218099.2:p.Asn313ThrfsTer13
ENST00000394090.2:c.824del	ENSP00000377650.2:p.Asn275ThrfsTer13
NM_000133.3:c.938del , LRG_556t1:c.938del	NP_000124.1:p.Asn313ThrfsTer13
NM_001313913.1:c.824del	NP_001300842.1:p.Asn275ThrfsTer13
XM_005262397.3:c.809del	XP_005262454.1:p.Asn270ThrfsTer13
XM_005262397.4:c.809del	XP_005262454.1:p.Asn270ThrfsTer13
NM_000133.4:c.938del MANE Select	NP_000124.1:p.Asn313ThrfsTer13
NM_001313913.2:c.824del	NP_001300842.1:p.Asn275ThrfsTer13