Canonical Allele Identifier: CA2695236161

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537076del , CM000685.2:g.139537076del	GRCh38
NC_000023.10:g.138619235del , CM000685.1:g.138619235del	GRCh37
NC_000023.9:g.138446901del	NCBI36
NG_007994.1:g.11341del , LRG_556:g.11341del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.155del MANE Select	ENSP00000218099.2:p.Leu52TrpfsTer?
ENST00000218099.6:c.155del	ENSP00000218099.2:p.Leu52TrpfsTer?
ENST00000394090.2:c.155del	ENSP00000377650.2:p.Leu52TrpfsTer?
ENST00000479617.2:n.162del
NM_000133.3:c.155del , LRG_556t1:c.155del	NP_000124.1:p.Leu52TrpfsTer?
NM_001313913.1:c.155del	NP_001300842.1:p.Leu52TrpfsTer?
XM_005262397.3:c.155del	XP_005262454.1:p.Leu52TrpfsTer?
XM_005262397.4:c.155del	XP_005262454.1:p.Leu52TrpfsTer?
NM_000133.4:c.155del MANE Select	NP_000124.1:p.Leu52TrpfsTer?
NM_001313913.2:c.155del	NP_001300842.1:p.Leu52TrpfsTer?