Canonical Allele Identifier: CA2695236194

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551173del , CM000685.2:g.139551173del	GRCh38
NC_000023.10:g.138633332del , CM000685.1:g.138633332del	GRCh37
NC_000023.9:g.138460998del	NCBI36
NG_007994.1:g.25438del , LRG_556:g.25438del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.632del MANE Select	ENSP00000218099.2:p.Leu211TrpfsTer?
ENST00000643157.1:n.1299del
ENST00000218099.6:c.632del	ENSP00000218099.2:p.Leu211TrpfsTer?
ENST00000394090.2:c.518del	ENSP00000377650.2:p.Leu173TrpfsTer?
NM_000133.3:c.632del , LRG_556t1:c.632del	NP_000124.1:p.Leu211TrpfsTer?
NM_001313913.1:c.518del	NP_001300842.1:p.Leu173TrpfsTer?
XM_005262397.3:c.503del	XP_005262454.1:p.Leu168TrpfsTer?
XM_005262397.4:c.503del	XP_005262454.1:p.Leu168TrpfsTer?
NM_000133.4:c.632del MANE Select	NP_000124.1:p.Leu211TrpfsTer?
NM_001313913.2:c.518del	NP_001300842.1:p.Leu173TrpfsTer?