Canonical Allele Identifier: CA915951980

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561896_139561897insGAGAT , CM000685.2:g.139561896_139561897insGAGAT	GRCh38
NC_000023.10:g.138644055_138644056insGAGAT , CM000685.1:g.138644055_138644056insGAGAT	GRCh37
NC_000023.9:g.138471721_138471722insGAGAT	NCBI36
NG_007994.1:g.36161_36162insGAGAT , LRG_556:g.36161_36162insGAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1211_1212insGAGAT MANE Select	ENSP00000218099.2:p.Asp405ArgfsTer2
ENST00000643157.1:n.1723+155_1723+156insGAGAT
ENST00000218099.6:c.1211_1212insGAGAT	ENSP00000218099.2:p.Asp405ArgfsTer2
ENST00000394090.2:c.1097_1098insGAGAT	ENSP00000377650.2:p.Asp367ArgfsTer2
NM_000133.3:c.1211_1212insGAGAT , LRG_556t1:c.1211_1212insGAGAT	NP_000124.1:p.Asp405ArgfsTer2
NM_001313913.1:c.1097_1098insGAGAT	NP_001300842.1:p.Asp367ArgfsTer2
XM_005262397.3:c.1082_1083insGAGAT	XP_005262454.1:p.Asp362ArgfsTer2
XM_005262397.4:c.1082_1083insGAGAT	XP_005262454.1:p.Asp362ArgfsTer2
NM_000133.4:c.1211_1212insGAGAT MANE Select	NP_000124.1:p.Asp405ArgfsTer2
NM_001313913.2:c.1097_1098insGAGAT	NP_001300842.1:p.Asp367ArgfsTer2