Canonical Allele Identifier: CA2695236373

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561863_139561874delinsCCATGTTCTGTA , CM000685.2:g.139561863_139561874delinsCCATGTTCTGTA	GRCh38
NC_000023.10:g.138644022_138644033delinsCCATGTTCTGTA , CM000685.1:g.138644022_138644033delinsCCATGTTCTGTA	GRCh37
NC_000023.9:g.138471688_138471699delinsCCATGTTCTGTA	NCBI36
NG_007994.1:g.36128_36139delinsCCATGTTCTGTA , LRG_556:g.36128_36139delinsCCATGTTCTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1178_1189delinsCCATGTTCTGTA MANE Select	ENSP00000218099.2:p.Asn393_Ala397delinsThrMetPheCysThr
ENST00000643157.1:n.1723+122_1723+133delinsCCATGTTCTGTA
ENST00000218099.6:c.1178_1189delinsCCATGTTCTGTA	ENSP00000218099.2:p.Asn393_Ala397delinsThrMetPheCysThr
ENST00000394090.2:c.1064_1075delinsCCATGTTCTGTA	ENSP00000377650.2:p.Asn355_Ala359delinsThrMetPheCysThr
NM_000133.3:c.1178_1189delinsCCATGTTCTGTA , LRG_556t1:c.1178_1189delinsCCATGTTCTGTA	NP_000124.1:p.Asn393_Ala397delinsThrMetPheCysThr
NM_001313913.1:c.1064_1075delinsCCATGTTCTGTA	NP_001300842.1:p.Asn355_Ala359delinsThrMetPheCysThr
XM_005262397.3:c.1049_1060delinsCCATGTTCTGTA	XP_005262454.1:p.Asn350_Ala354delinsThrMetPheCysThr
XM_005262397.4:c.1049_1060delinsCCATGTTCTGTA	XP_005262454.1:p.Asn350_Ala354delinsThrMetPheCysThr
NM_000133.4:c.1178_1189delinsCCATGTTCTGTA MANE Select	NP_000124.1:p.Asn393_Ala397delinsThrMetPheCysThr
NM_001313913.2:c.1064_1075delinsCCATGTTCTGTA	NP_001300842.1:p.Asn355_Ala359delinsThrMetPheCysThr