Canonical Allele Identifier: CA2695236420

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562027del , CM000685.2:g.139562027del	GRCh38
NC_000023.10:g.138644186del , CM000685.1:g.138644186del	GRCh37
NC_000023.9:g.138471852del	NCBI36
NG_007994.1:g.36292del , LRG_556:g.36292del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1342del MANE Select	ENSP00000218099.2:p.Ser448ProfsTer?
ENST00000643157.1:n.1723+286del
ENST00000218099.6:c.1342del	ENSP00000218099.2:p.Ser448ProfsTer?
ENST00000394090.2:c.1228del	ENSP00000377650.2:p.Ser410ProfsTer?
NM_000133.3:c.1342del , LRG_556t1:c.1342del	NP_000124.1:p.Ser448ProfsTer?
NM_001313913.1:c.1228del	NP_001300842.1:p.Ser410ProfsTer?
XM_005262397.3:c.1213del	XP_005262454.1:p.Ser405ProfsTer?
XM_005262397.4:c.1213del	XP_005262454.1:p.Ser405ProfsTer?
NM_000133.4:c.1342del MANE Select	NP_000124.1:p.Ser448ProfsTer?
NM_001313913.2:c.1228del	NP_001300842.1:p.Ser410ProfsTer?