Canonical Allele Identifier: CA2695236380

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548425_139548426insC , CM000685.2:g.139548425_139548426insC	GRCh38
NC_000023.10:g.138630584_138630585insC , CM000685.1:g.138630584_138630585insC	GRCh37
NC_000023.9:g.138458250_138458251insC	NCBI36
NG_007994.1:g.22690_22691insC , LRG_556:g.22690_22691insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.454_455insC MANE Select	ENSP00000218099.2:p.Lys152ThrfsTer8
ENST00000643157.1:n.1121_1122insC
ENST00000218099.6:c.454_455insC	ENSP00000218099.2:p.Lys152ThrfsTer8
ENST00000394090.2:c.340_341insC	ENSP00000377650.2:p.Lys114ThrfsTer8
NM_000133.3:c.454_455insC , LRG_556t1:c.454_455insC	NP_000124.1:p.Lys152ThrfsTer8
NM_001313913.1:c.340_341insC	NP_001300842.1:p.Lys114ThrfsTer8
XM_005262397.3:c.392-2637_392-2636insC	XP_005262454.1:n.392-2637_392-2636insC
XM_005262397.4:c.392-2637_392-2636insC	XP_005262454.1:n.392-2637_392-2636insC
NM_000133.4:c.454_455insC MANE Select	NP_000124.1:p.Lys152ThrfsTer8
NM_001313913.2:c.340_341insC	NP_001300842.1:p.Lys114ThrfsTer8