Canonical Allele Identifier: CA2695236146

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537017del , CM000685.2:g.139537017del	GRCh38
NC_000023.10:g.138619176del , CM000685.1:g.138619176del	GRCh37
NC_000023.9:g.138446842del	NCBI36
NG_007994.1:g.11282del , LRG_556:g.11282del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.96del MANE Select	ENSP00000218099.2:p.Asp33IlefsTer9
ENST00000218099.6:c.96del	ENSP00000218099.2:p.Asp33IlefsTer9
ENST00000394090.2:c.96del	ENSP00000377650.2:p.Asp33IlefsTer9
ENST00000479617.2:n.103del
NM_000133.3:c.96del , LRG_556t1:c.96del	NP_000124.1:p.Asp33IlefsTer9
NM_001313913.1:c.96del	NP_001300842.1:p.Asp33IlefsTer9
XM_005262397.3:c.96del	XP_005262454.1:p.Asp33IlefsTer9
XM_005262397.4:c.96del	XP_005262454.1:p.Asp33IlefsTer9
NM_000133.4:c.96del MANE Select	NP_000124.1:p.Asp33IlefsTer9
NM_001313913.2:c.96del	NP_001300842.1:p.Asp33IlefsTer9