Canonical Allele Identifier: CA2695236307

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561670_139561671insCTAAGTGCTAAACA , CM000685.2:g.139561670_139561671insCTAAGTGCTAAACA	GRCh38
NC_000023.10:g.138643829_138643830insCTAAGTGCTAAACA , CM000685.1:g.138643829_138643830insCTAAGTGCTAAACA	GRCh37
NC_000023.9:g.138471495_138471496insCTAAGTGCTAAACA	NCBI36
NG_007994.1:g.35935_35936insCTAAGTGCTAAACA , LRG_556:g.35935_35936insCTAAGTGCTAAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.985_986insCTAAGTGCTAAACA MANE Select	ENSP00000218099.2:p.Ser329ThrfsTer4
ENST00000643157.1:n.1652_1653insCTAAGTGCTAAACA
ENST00000218099.6:c.985_986insCTAAGTGCTAAACA	ENSP00000218099.2:p.Ser329ThrfsTer4
ENST00000394090.2:c.871_872insCTAAGTGCTAAACA	ENSP00000377650.2:p.Ser291ThrfsTer4
NM_000133.3:c.985_986insCTAAGTGCTAAACA , LRG_556t1:c.985_986insCTAAGTGCTAAACA	NP_000124.1:p.Ser329ThrfsTer4
NM_001313913.1:c.871_872insCTAAGTGCTAAACA	NP_001300842.1:p.Ser291ThrfsTer4
XM_005262397.3:c.856_857insCTAAGTGCTAAACA	XP_005262454.1:p.Ser286ThrfsTer4
XM_005262397.4:c.856_857insCTAAGTGCTAAACA	XP_005262454.1:p.Ser286ThrfsTer4
NM_000133.4:c.985_986insCTAAGTGCTAAACA MANE Select	NP_000124.1:p.Ser329ThrfsTer4
NM_001313913.2:c.871_872insCTAAGTGCTAAACA	NP_001300842.1:p.Ser291ThrfsTer4