Canonical Allele Identifier: CA2823819669

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561668del , CM000685.2:g.139561668del	GRCh38
NC_000023.10:g.138643827del , CM000685.1:g.138643827del	GRCh37
NC_000023.9:g.138471493del	NCBI36
NG_007994.1:g.35933del , LRG_556:g.35933del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.983del MANE Select	ENSP00000218099.2:p.Asn328ThrfsTer26
ENST00000643157.1:n.1650del
ENST00000218099.6:c.983del	ENSP00000218099.2:p.Asn328ThrfsTer26
ENST00000394090.2:c.869del	ENSP00000377650.2:p.Asn290ThrfsTer26
NM_000133.3:c.983del , LRG_556t1:c.983del	NP_000124.1:p.Asn328ThrfsTer26
NM_001313913.1:c.869del	NP_001300842.1:p.Asn290ThrfsTer26
XM_005262397.3:c.854del	XP_005262454.1:p.Asn285ThrfsTer26
XM_005262397.4:c.854del	XP_005262454.1:p.Asn285ThrfsTer26
NM_000133.4:c.983del MANE Select	NP_000124.1:p.Asn328ThrfsTer26
NM_001313913.2:c.869del	NP_001300842.1:p.Asn290ThrfsTer26