Canonical Allele Identifier: CA2582342933

Gene: F9

Linked Data

• ClinVar Variation Id: 2581701
• ClinVar RCV Id: RCV003330477

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561771del , CM000685.2:g.139561771del	GRCh38
NC_000023.10:g.138643930del , CM000685.1:g.138643930del	GRCh37
NC_000023.9:g.138471596del	NCBI36
NG_007994.1:g.36036del , LRG_556:g.36036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1086del MANE Select	ENSP00000218099.2:p.Arg364AspfsTer4
ENST00000643157.1:n.1723+30del
ENST00000218099.6:c.1086del	ENSP00000218099.2:p.Arg364AspfsTer4
ENST00000394090.2:c.972del	ENSP00000377650.2:p.Arg326AspfsTer4
NM_000133.3:c.1086del , LRG_556t1:c.1086del	NP_000124.1:p.Arg364AspfsTer4
NM_001313913.1:c.972del	NP_001300842.1:p.Arg326AspfsTer4
XM_005262397.3:c.957del	XP_005262454.1:p.Arg321AspfsTer4
XM_005262397.4:c.957del	XP_005262454.1:p.Arg321AspfsTer4
NM_000133.4:c.1086del MANE Select	NP_000124.1:p.Arg364AspfsTer4
NM_001313913.2:c.972del	NP_001300842.1:p.Arg326AspfsTer4